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甘蓝型油菜根系形态对低磷胁迫的反应及其QTL分析
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摘要
油菜是我国的主要油料作物之一,种植面积和总产均居世界首位。位于长江中下游的甘蓝型油菜主产区磷素缺乏,而甘蓝型油菜对缺磷敏感,限制了此产区油菜产量的提高。通过遗传育种的方法,开发和培育高效吸收利用磷营养的油菜品种具有很好的发展前景。根系形态构型的适应性变化是植物响应低磷胁迫的重要机制。为阐明油菜磷高效遗传特性,本研究以磷高效亲本鄂油长角和磷低效亲本B104-2所构建的重组自交系(命名为BE-RILs,F10)为材料,采用纸培试验,调查了高磷和低磷条件下BE-RILs的苗期干物重,磷含量和根系形态性状。在利用SSR、AFLP、SRAP等分子标记所构建的遗传连锁图谱的基础上,对BE-RILs表型性状进行数量遗传位点(QTL)的定位,并利用QTL元分析和比较作图对油菜适应低磷胁迫的遗传机制进行了解析。主要结果如下:
     1甘蓝型油菜磷效率遗传连锁图的构建及与拟南芥基因组的比较作图分析以BE-RILs各株系的基因组DNA为模板,利用SSR、AFLP、SRAP等分子标记分析群体株系基因型,通过作图软件Jionmap4.0,构建了一张含有553个分子标记的遗传连锁图,包括202个SSR,62个AFLP,234个SRAP和55个功能标记。此遗传连锁图长度为1592.7 cM,两相邻标记的平均距离为2.9 cM。利用BE-RILs遗传图谱上已知序列信息的标记作为锚定标记,将该遗传图谱与拟南芥基因组进行比较作图分析,在BE-RILs遗传图谱的10个连锁群的部分区段定位了27个保守区段。
     2布置三次纸培试验,调查两亲本和BE-RILs在高磷和低磷条件下的表型性状设计以蓝色无磷吸水纸为支撑的纸培系统,在根系收获后,利用WinRhizo根系分析软件测定根系总根长,根系表面积,根体积和平均根系直径,同时测定植株干重和磷含量。结果发现,在低磷条件下,相对于磷低效亲本B104-2,磷高效亲本鄂油长角不但形成了较大根系系统,而且吸收了较多磷和生成了较多干物质,但有较低的磷利用效率。说明鄂油长角的高效机制在于低磷条件下形成发达根系,从而获得较多磷和形成较高干物质。BE-RILs群体各表型性状在低磷和高磷条件下均呈连续的分布,并存在着广泛的变异,变异系数处于20.5-40.6%之间,这表明BE-RILs群体的双亲对这些性状所贡献的等位基因在其后代群体中有广泛的分离。
     3磷效率QTL的检测和分析’
     3.1两个磷水平下苗期各性状显著性QTL检测利用Wincart2.5的复合区间作图法对三次纸培试验两个磷水平下的地上部干重,根系干重,总干重,根冠比,总根长,根系表面积,平均根系直径,根体积,根尖数,磷含量,磷吸收累积量和磷利用效率12个性状进行了QTL定位。共检测到136个显著性QTL,其中高磷条件下63个和低磷条件下73个。这些QTL主要集中分布在A1, A3, A6, C1, C2, C3, C6和C8这8个连锁群上,单个QTL解释的表型遗传变异率在7.95%-22.00%之间。
     3.2磷效率QTL的整合对置信区间重叠的显著性QTL利用QTL元分析软件进行整合。首先对同一性状在不同试验中重叠显著性QTL进行整合,得到94个(高磷44个和低磷50)一致性QTL。第二步对不同性状相互重叠的一致性QTL进行整合,得到37个特异性QTL,包括高磷特异的QTL 10个,低磷特异的QTL 15个,稳定表达的QTL 12个。
     3.3功能标记在QTL区间的分布有10个功能标记定位在特异性QTL的置信区间内,低磷特异QTL置信区间内的有5个,高磷特异QTL置信区间内的只有1个,其他4个位于稳定表达的QTL置信区间内。这5个位于低磷特异QTL区间内的标记为BnSQD1-C1, BnGPT2-C1, BnPHO1-C1, BnIPS2-C3和BnGPT1-C3,其相应的低磷特异QTL为uq.C1a, uq.C1b, uq.C1b, uq.C3a和uq.C3c。利用这些低磷特异QTL区间内的标记对BE-RILs各株系进行筛选,得到聚合不同优良等位基因的株系。
     3.4同源基因在BE-RILs图谱上的in silico定位在完成与拟南芥基因组比较作图的基础上,把拟南芥中423个磷代谢途径相关基因,响应低磷胁迫的转录因子,根系发育和激素传导相关基因的位置信息,用电子作图方法定位在BE-RILs遗传图谱的810个基因座位上,其中67个基因位于特异性QTL区间所对应的保守区段内,预测为QTL候选基因。这些QTL信息和候选基因为解析油菜适应低磷胁迫机制奠定了基础,为下一步定位克隆这些基因提供了丰富的信息。
Rapeseed is one of the major oilseed crops in China, and planting area and total yield are the first in the world. The middle and lower valley of the Yangtze River in South China is the largest cultivated region for rapeseed (Brassica napus), where the soil available P concentration is usually lower. B. napus has high P requirement for its optimal seed yield and quality, so low available P concentration in soils seriously limits the production of B. napus in this area. Exploiting or breeding P-efficient cultivars has become an attractive prospect for rapeseed production. Modification of root morphology and architecture is the key adaptive strategy of plant in response to P deficiency. In this study, a B. napus F10 recombinant inbred lines (was named as BE-RILs) population, which developed from a cross between P-efficient rapeseed cv. Eyou Changjia and P-inefficient cv. B104-2, was employed to investigate plant dry weight, P concentration, and root morphology traits at the seedling stage under high P (HP) and low P (LP) conditions in paper culture experiments. Based on a genetic linkage map constructed with SSR, AFLP, SRAP markers, quantitative trait loci (QTL) for these traits were identified, and the genetic basis of P-efficiency was dissected through QTL meta-analysis and comparative mapping method.
     The main results were as follows:
     1 Constructing a genetic linkage map for P efficiency in B. napus and comparative mapping with Arabidopsis Used genomes DNA of BE-RILs as template, the genotypes were analyzed with SSR, AFLP, SRAP markers. A genetic linkage map with 553 molecular markers was constructed by Jionmap4.0, including 202 SSR,62 AFLP,234 SRAP and 55 functional markers. The total genetic distance was 1592.7 centimorgans (cM) and an average distance was 2.9 cM between adjacent markers. Futhermore, the comparative genomics analysis between B. napus and Arabidopsis was mapped employing SSR markers with known sequence information as anchored markers. And 27 synteny blocks were aligned with some regions of ten linkage groups of BE-RILs.
     2 Investigating the phenotypic traits of two parents and BE-RILs under HP and LP conditions by three independent paper culture experiments The paper culture system which employed P-free blue germination paper as support was designed to investigate the phenotypic traits. After harvesting, total root length of plant, root surface area, root volume, and root average diameter were analyzed with WinRhizo root image analysis software. Plant dry weight and plant P concentration were also detected. As results, under low P condition, compared to the P-inefficient parent B104-2, the P-efficient parent Eyou Changjia not only developed bigger root system, but also produced higher biomass and acquired more P. However, Eyou Changjia had lower P use efficiency. This suggested that high P efficiency of Eyou Changjia was mainly attributed to developed root system. The phenotypic traits showed continuous distribution in BE-RILs. The coefficients of variation (CV) for these traits ranged from 20.5% to 40.6%. This indicated that each parent possesses alleles that have both positive and negative effects on the traits.
     3 Detecting and analyzing the QTL of P efficiency
     3.1 Detecting the significant-QTL for various traits under two P conditions QTL for twelve traits-SDW, RDW, TDW, RSR, RL, RSA, RD, TIP, PC, PU, and PUE under HP and LP conditions were detected in the three experiments using the composite interval method by Wincart2.5 software. As results, a total of 136 significant-QTL were identified, where 63 and 73 QTL were detected for HP and LP condition, respectively. These significant-QTL were distributed on eight linkage groups-A1, A3, A6, C1, C2, C3, C6 and C8. The contribution to phenotypic variations for the single QTL ranged from 7.95%-22.00%.
     3.2 Meta-analysis QTL of P efficiency The overlapping QTL for the traits in different experiments were integrated using QTL meta-analysis. First, the overlapping significant-QTL for the same traits in different experiments were integrated, and were got 94 consensus-QTL, which included 44 for HP and 50 for LP, respectively. Second, the overlapping consensus-QTL for different traits were integrated into 37 unique-QTL, which included 10 QTL specific for HP,15 QTL specific for LP and 12 constitutive QTL, respectively.
     3.3 Distributing of functional markers in the confidence intervals of unique-QTL 10 functional markers were distributed in the confidence intervals of unique-QTL. Five markers were located in the intervals of LP-specific QTL. One marker was located in the interval of HP-specific QTL. Four markers were located in the intervals of constitutive QTL. The five markers located in the intervals of LP-specific QTL were BnSQDl-Cl, BnGPT2-C1, BnPHO1-C1, BnIPS2-C3 and BnGPT1-C3, which correspond to LP-specific QTL uq.C1a, uq.C1b, uq.C1b, uq.C3a and uq.C3c. Some RI lines pyramiding favorable alleles were found using these functional makers in the intervals of LP-specific QTL
     3.4 Locating the orthologous genes of Arabidopsis on BE-RILs linkage map by in silico mapping On the basis of comparative genomics between B. napus and Arabidopsis,423 orthologous genes for P metabolism, P-responsive transcription factors, root development and auxin transporter in Arabidopsis were located on 850 loci of BE-RILs linkage map by in silico mapping, and 67 orthologous genes were corresponded to the intervals of QTL, which were speculated as the candidate genes of QTL in B. napus. These information of QTL and candidate genes provide a solid foundation for improving the adaptability of P deficiency, and paves the way for map-based cloning of these genes.
引文
1. 方宣钧,吴为人,唐纪良.作物DNA标记辅助育种,北京:科学出版社,2000
    2. 关强,张月学,徐香玲,等.DNA分子标记的研究进展及几种新型分子标记技术.黑龙江农业科学,2008,1:102-104
    3. 韩毅强.甘蓝型油菜磷营养高效基因的定位和分析.[硕士学位论文].武汉:华中农业大学图书馆,2004
    4. 石磊,梁宏玲,徐芳森,等.甘蓝型油菜幼苗体内磷组分差异与磷高效关系的研究.植物营养与肥料学报,2008,14(2):351-356
    5. 王汉中.中国油料产业发展的现状、问题与对策.中国油料作物学报,2005,4:100-105
    6. 薛永国,刘丽君,高明杰,等.作物中QTL的研究进展及展望.东北农业大学学报,2007,38:542-547.
    7. Akhtar MS, Oki Y, Adachi T. Intraspecific variations of phosphorus absorption and remobilization, P forms, and their internal buffering in Brassica cultivars exposed to a P-stressed environment. J Integr Plant Biol,2008,50:703-716
    8. Araujo AP, Antunes IF, Teixeira MG. Inheritance of root traits and phosphorus uptake in common bean (Phaseolus vulgaris L.) under limited soil phosphorus supply. Euphytica,2005,145:33-40
    9. Arcade A, Labourdette A, Falque M, et al. BioMercator:integrating genetic maps and QTL towards discovery of candidate genes. Bioinformatics,2004, 20:2324-2326
    10. Aung K, Lin S, Wu C, et al. pho2, a phosphate overaccumulator, is caused by a nonsense mutation in a microRNA399 target gene. Plant Physiol,2006,141: 1000-1011
    11. Batjes NH. A world dataset of derived soil properties by FAO-UNESCO soil unit for global modelling. Soil Use Manage,1997,13:9-16
    12. Beebe SE, Rojas-Pierce M, Yan X, et al. Quantitative trait loci for root architecture traits correlated with phosphorus acquisition in common bean. Crop Sci,2006, 46:413-423
    13. Bengough AG, Gordon DC, Al-Menaie H, et al. Gel observation chamber for rapid screening of root traits in cereal seedlings. Plant Soil,2004,262:63-70
    14. Bonser AM, Lynch J, Snapp S. Effect of phosphorus deficiency on growth angle of basal roots in Phaseolus vulgaris. New Phytol,1996,132:281-288.
    15. Borch K, Bouma TJ, Lynch JP, et al. Ethylene:a regulator of root architectural responses to soil phosphorus availability. Plant, Cell & Environ,1999,22:425-431
    16. Burleigh SH, Harrison MJ. A novel gene whose expression in Medicago truncatula roots is suppressed in response to colonization by vesicular-arbuscular mycorrhizal (VAM) fungi and to phosphate nutrition. Plant Mol Biol,1997,34:199-208
    17. Carpenter SR. Phosphorus control is critical to mitigating eutrophication. Proc Natl Acad Sci USA,2008,105:11039-11040
    18. Chardon F, Virlon B, Moreau L, et al. Genetic architecture of flowering time in maize as inferred from quantitative trait loci meta-analysis and synteny conservation with the rice genome. Genetics,2004,168:2169-2185
    19. Chen W, Zhang Y, Liu X, et al. Detection of QTL for six yield-related traits in oilseed rape (Brassica napus) using DH and immortalized F2 populations. Theor Appl Genet,2007,115:849-858
    20. Chen XM, Xu JS, Xia S, et al. Development and genetic mapping of micro satellite markers from genome survey sequences in Brassica napus. Theor Appl Genet, 2009a,118:1121-1131
    21. Chen YF, Li LQ, Xu Q, et al. The WRKY6 transcription factor modulates PHOSPHATE1 expression in response to low Pi stress in Arabidopsis. The Plant Cell,2009b, doi/10.1105/tpc.108.064980
    22. Cheung WY, Friesen L, Rakow GFW, et al. A RFLP-based linkage map of mustard (Brassica juncea L.). Theor Appl Genet,1997,94:841-851
    23. Chiou T, Aung K, Lin S, et al. Regulation of phosphate homeostasis by microRNA in Arabidopsis. Plant Cell,2006,18:412-421
    24. Churchill GA, Doerge RW. Empirical threshold values for quantitative trait mapping. Genetics,1994,138:963-971
    25. De Dorlodot S, Forster B, Pages L, et al. Root system architecture:opportunities and constraints for genetic improvement of crops. Trends Plant Sci,2007, 12:474-481
    26. Devaiah BN, Karthikeyan AS. Raghothama K G. WRKY75 transcription factor is a modulator of phosphate acquisition and root development in Arabidopsis. Plant Physiol,2007,143:1789-1801.
    27. Dong B, Rengel Z, Delhaize E. Uptake and translocationof phosphate by pho2 mutant and wild-type seedlings of Arabidopsis thaliana. Plant Physiol,1998,205, 251-256.
    28. Doyle JJ, Doyle JL. Isolation of plant DNA from fresh tissue. Focus,1990,12:13-15
    29. Duan H, Shi L, Ye X, et al. Identification of phosphorous efficient germplasm in oilseed rape. J Plant Nutri,2009,32:1148-1163
    30. Essigmann B, Guler S, Narang RA, et al. Phosphate availability affects the thylakoid lipid composition and the expression of SQD1, a gene required for sulfolipid biosynthesis in Arabidopsis thaliana. Proc Natl Acad Sci USA,1998, 95:1950-1955
    31. Fageria NK, Baligar VC, Li YC. The role of nutrient efficient plants in improving crop yields in the twenty first century. J Plant Nutri,2008,31:1121-1157
    32. Franco-Zorrilla JM, Martin AC, Leyva A, et al. Interaction between phosphate-starvation, sugar, and cytokinin signaling in Arabidopsis and the roles of cytokinin receptors CRE1/AHK4 and AHK3. Plant Physiol,2005,138:847-857
    33. Frary A, Nesbitt TC, Grandillo S, et al.fw2.2:a quantitative trait locus key to the evolution of tomato fruit size. Science,2000,289:85-88
    34. Fujii H, Chiou TJ, Lin SI, et al. A miRNA involved in phosphate-starvation response in Arabidopsis. Curr Biol,2005,15:2038-2042
    35. Gahoonia TS, Nielsen NE. Barley genotypes with long root hairs sustain high grain yields in low-P field. Plant Soil 2004,262:55-62
    36. Gahoonia TS, Nielsen NE. Direct evidence on participation of root hairs in phosphorus (32P) uptake from soil. Plant Soil,1998,198:147-152
    37. Gahoonia TS, Nielsen NE. Phosphorus (P) uptake and growth of a root hairless barley mutant (bald root barley, brb) and wild type in low-and high-P soils. Plant, Cell &Environ,2003,26:1759-1766
    38. Gao M, Li G, Yang B, et al. High-density Brassica oleracea linkage map: identification of useful new linkages. Theor Appl Genet,2007,115:277-287
    39. German MA, Pillay M, Jeong DH, et al. Global identification of microRNA-target RNA pairs by parallel analysis of RNA ends. Nat Biotechnol,2008,26:941-946
    40. Gilbert GA, Knight JD, Vance CP, et al. Proteoid root development of phosphorus deficient lupin is mimicked by auxin and phosphonate. Ann Bot,2000,85:921-928
    41. Glassop D, Smith SE, Smith FW. Cereal phosphate transporters associated with the mycorrhizal pathway of phosphate uptake into roots. Planta,2005,222:688-698
    42. Gonzalez E, Solano R, Rubio V, et al. PHOSPHATE TRANSPORTER TRAFFIC FACILITATOR1 is a plant-specific SEC12-related protein that enables the endoplasmic reticulum exit of a high-affinity phosphate transporter in Arabidopsis. Plant Cell,2005,17:3500-3512
    43. Gupta V, Mukhopadhyay A, Arumugam N, et al. Molecular tagging of erucic acid trait in oilseed mustard (Brassica juncea) by QTL mapping and single nucleotide polymorphisms in FAE1 gene. Theor Appl Genet,2004,108:743-749
    44. Hacket CA, Breadfoot LB. Effects of genotyp ing errors, missing values and segregation distortion in molecular marker data on the construction of linkage maps. Heredity,2003,90:33-38
    45. Hagstrom J. James WM, Skene KR. A comparison of structure, development and function in cluster roots of Lupinus albus L. under phosphate and iron stress. Plant Soil,2001,232:81-90
    46. Hamburger D, Rezzonico E, MacDonald-Comber Petetot J, et al. Identification and characterization of the Arabidopsis PHO1 gene involved in phosphate loading to the xylem. Plant Cell,2002,14:889-902
    47. Hammond JP, Bennett MJ, Bowen HC, et al. Changes in gene expression in Arabidopsis shoots during phosphate starvation and the potential for developing smart plants. Plant Physiol,2003,132:578-596
    48. Hammond JP, Broadley MR, White PJ, et al. Shoot yield drives phosphorus use efficiency in Brassica oleracea and correlates with root architecture traits. J Exp Bot, 2009,60:1953-1968
    49. Hammond JP, White PJ. Sucrose transport in the phloem:integrating root responses to phosphorus starvation. J Exp Bot,2008,59:93-109
    50. He CJ, Morgan PW, Drew M. Enhanced sensitivity to ethylene in nitrogen-or phosphate-starved Roots of Zea mays L. during Aerenchyma Formation. Plant Physiol,1992,98:137-142
    51. He Y, Liao H, Yan X. Localized supply of phosphorus induces root morphological and architectural changes of rice in split and stratified soil cultures. Plant Soil,2003, 248:247-256
    52. Hermans C, Hammond JP, White PJ, et al. How do plants respond to nutrient shortage by biomass allocation? Trends Plant Sci,2006,11:610-617
    53. Heuer S, Lu X, Chin JH, et al. Comparative sequence analyses of the major quantitative trait locus phosphorus uptake 1 (Pupl) reveal a complex genetic structure. Plant Biotechnol J,2009,7:456-471
    54. Holford ICR. Soil phosphorus:its measurement, and its uptake by plants. Aust J Soil Res,1997,35:227-239
    55. Hossain MA, Khan MSA, Nasreen S, et al. Effect of seed size and phosphorus fertilizer on root length density, P uptake, day matter production and yield of groundnut. J Agric Res,2006,44:127-137
    56. Hou XL, Wu P, Jiao FC, et al. Regulation of the expression of OsIPS1 and OsIPS2 in rice via systemic and local Pi signalling and hormones. Plant, Cell & Environ, 2005,28:353-364
    57. Ishimaru K, Ono K, Kashiwagi T. Identification of a new gene controlling plant height in rice using the candidate-gene strategy. Planta,2004,218:388-395
    58. Ismail A, Heuer S, Thomson M, et al. Genetic and genomic approaches to develop rice germplasm for problem soils. Plant Mol Biol,2007,65:547-570
    59. Jain A, Poling MD, Karthikeyan AS, et al. Differential effects of sucrose and auxin on localized phosphate deficiency-induced modulation of different traits of root system architecture in Arabidopsis. Plant Physiol,2007a,144:232-247
    60. Jain A, Vasconcelos MJ, Raghothama KG. Molecular mechanisms of plant adaptation to phosphate deficiency. In:Janick J ed, Plant breeding reviews,2007b, vol 29. Wiley, NJ,pp 359-419
    61. Kao CH, Zeng ZB, Teasdale RD. Multiple interval mapping for quantitative trait loci. Genetics,1999,152:1203-1216
    62. Keerthisinghe G, Hocking PJ, Ryan PR, et al. Effect of phosphrous supply on the formation and function of proteoid roots of white lupin (Lupinus albus L.). Plant, Cell &Environ,1998,21:467-478
    63. Kelly AA, Dormann P. DGD2, an Arabidopsis gene encoding a UDP-galactose-dependent digalactosyldiacylglycerol synthase is expressed during growth under phosphate-limiting conditions. J Biol Chem,2002,277:1166-1173
    64. Kojima S, Takahashi Y, Kobayashi Y, et al. Hd3a, a rice ortholog of the Arabidopsis FT gene, promotes transition to flowering downstream of Hdl under short-day conditions. Plant Cell Physiol,2002,43:1096-1105
    65. Konishi S, Izawa T, Lin SY, et al. An SNP caused loss of seed shattering during rice domestication. Science,2006,312:1392-1396
    66. Lander E S, Green P, Abrahamson J, et al. Mapmaker:an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. Genomics,1987,1:174-181.
    67. Landry BS, Hubert N. A genetic map of Brassica napus based on restriction fragment length polymorphisms detected with expressed DNA sequences. Genome, 1991,34:543-552
    68. Li G, Quiros CF. Sequence-related amplified polymorphism (SRAP), a new marker system based on a simple PCR reaction:its application to mapping and gene tagging in Brassica. Theor Appl Genet,2001,103:455-461
    69. Li J, Xie Y, Dai A, et al. Root and shoot traits responses to phosphorus deficiency and QTL analysis at seedling stage using introgression lines of rice. J Genet Genomics,2009,36:173-183
    70. Li M, Qin C, Welti R, et al. Double knockouts of phospholipases Dzl and Dz2 in Arabidopsis affect root elongation during phosphate-limited growth but do not affect root hair patterning. Plant Physiol,2006,140:761-770
    71. Li YD, Wang YJ, Tong YP, et al. QTL mapping of phosphorus deficiency tolerance in soybean (Glycine max L. Merr.). Euphytica,2005,142:137-142
    72. Li YY, Shen JX, Wang TH, et al. QTL analysis of yield-related traits and their association with functional markers in Brassica napus L. Aust J Agr Res,2007,58 (8):759-766.
    73. Liao H, Rubio G, Yan X, et al. Effect of phosphorus availability on basal root shallowness in common bean. Plant Soil,2001,232:69-79
    74. Lin SI, Chiang SF, Lin WY, et al. Regulatory network of microRNA399 and PHO2 by systemic signaling. Plant Physiol,2008,147:732-746
    75. Liu CM, Muchhal US, Uthappa M, et al. Tomato phosphate transporter genes are differentially regulated in plant tissues by phosphorus. Plant Physiol,1998, 116:91-99
    76. Liu Y, Mi GH, Chen FJ, et al. Rhizosphere effect and root growth of two maize(Zea mays L.) genotypes with constrasting P efficiency at low P availability. Plant Sci, 2004,167:217-223.
    77. Lloyd JC, Zakhlenluk OV. Responses of primary and secondary metabolism to sugra accumulation revealed by microarray expression analysis of the Arabidopsis mutant,pho3. J Exp Bot,2004,55:1221-1230
    78. Loes AK, Gahoonia TS. Genetic variation in specific root length in Scandinavian wheat and barley accessions. Euphytica,2004,137:243-249
    79. Lombard V, Delourme R A. Consensus linkage map for rapeseed(Brassica napus L.):construction and integration of three individual maps from DH population. Theor Appl Genet,2001,103:491-507.
    80. Long Y, Shi JQ, Qiu D, et al. Flowering time quantitative trait loci analysis of oilseed Brassica in multiple environments and genomewide alignment with Arabidopsis. Genetics,2007,177:2433-2444
    81. Lopez-Bucio J, Hernandez-Abreu E, Sanchez-Calderon L, et al. Phosphate availability alters architecture and causes changes in hormone sensitivity in the Arabidopsis root system. Plant Physiol,2002,129:1-13
    82. Lopez-Bucio J, Hernandez-Abreu E, Sanchez-Calderon L, et al. An auxin transport independent pathway is involved in phosphate stress-induced root architectural alterations in Arabidopsis. Identification of BIG as a mediator of auxin in pericycle cell activation. Plant Physiol,2005,137:681-691
    83. Lorieux M, Ndjiondjop MN, Ghesquiere A. A first interspecific Oryza sativa × Oryza glaberrima micro satellite-based genetic linkage map. Theor Appl Genet, 2000,100:593-601
    84. Louis I, Racette S, Torrey JG. Occurrence of cluster roots on myrica cerifera L (myricaceae) in water culture in relation to phosphorus nutrition. New Phytol,1990, 115:311-317
    85. Lowe A, Moule C, Trick M, et al. Efficient large-scale development of microsatellites for marker and mapping applications in Brassica crop species. Theor Appl Genet,2004,108:1103-1112
    86. Lu H, Romero-Severson J, Bernardo R. Chromosomal regions associated with segregation distortion in maize. Theor Appl Genet,2002,105:622-628
    87. Lynch JP. Roots of the second green revolution. Aust J Bot,2007,55:493-512
    88. Ma Z, Baskin TL, Brown KM, et al. Regulation of root elongation under phosphorus stress involves changes in ethylene responsiveness. Plant Physiol,2003, 131:1381-1390
    89. Ma Z, Bielenberg DG, Brown KM, et al. Regulation of root hair density by phosphorus availability in Arabidopsis thaliana. Plant, Cell & Environ 2001a, 24:459-467
    90. Ma Z, Walk TC, Marcus A, et al. Morphological synergism in root hair length, density, initiation and geometry for phosphorus acquisition in Arabidopsis thaliana: A modeling approach. Plant Soil,2001b,236:221-235
    91. Marschnera P, Solaimana Z, Rengel Z. Brassica genotypes differ in growth, phosphorus uptake and rhizosphere properties under P-limiting conditions. Soil Biol Biochem,2007,39:87-98
    92. Martin AC, del Pozo JC, Iglesias J, et al. Influence of cytokinins on the expression of phosphate starvation responsive genes in Arabidopsis. Plant J,2000,24:559-567
    93. Ming F, Zhang X, Mi G, et al. Identification of quantitative trait loci affecting tolerance to low phosphorus in rice(Oryza Sativa L.). Chinese Sci Bull,2000, 45:520-525
    94. Misson J, Thibaud MC, Bechtold N, et al. Transcriptional regulation and functional properties of Arabidopsis Pht1;4, a high affinity transporter contributing greatly to phosphate uptake in phosphate deprived plants. Plant Mol Biol,2004,55:727-741
    95. Muchhal US, Pardo JM, Raghathama KG. Phosphate transporter from higher plant Arabidopsis thaliana. Proc Natl Acad Sci USA,1996,93:10519-10523
    96. Mudge SR, Rae AL, Diatloff E, et al. Expression analysis suggests novel roles for members of the Phtl family of phosphate transporters in Arabidopsis. Plant J,2002, 31:341-353
    97. Mukatira UT, Liu C, Varadarajan DK, et al. Negative regulation of phosphate starvation-induced genes. Plant Physiol,2001,127:1854-1862
    98. Nacry P, Canivenc G, Muller B, et al. A role for auxin redistribution in the responses of the root system architecture to phosphate starvation in Arabidopsis. Plant Physiol, 2005,138:2061-2074
    99. Nagy R, Karandashov V, Chague W, et al. The characterization of novel mycorrhiza-specific phosphate transporters from Lycopersicon esculentum and Solanum tuberosum uncovers functional redundancy in symbiotic phosphate transport in solanaceous species. Plant J,2005,42:236-250
    100. Neeraja C, Maghirang-Rodriguez R, Pamplona A, et al. A marker-assisted backcross approach for developing submergence-tolerant rice cultivars. Theor Appl Genet, 2007,115:767-776
    101. Neumann GN, Massonneau AS, Langlade N, et al. Physiological aspects of cluster root function and development in phosphorus-deficient white Lupin (Lupinus albus L.). Ann Bot,2000,85:909-919
    102. Ni JJ, Wu P, Senadhira D, Huang N. Mapping QTLs for phosphorus deficiency tolerance in rice (Oryza sativa L.). Theor Appl Genet,1998,97:1361-1369
    103. Ni JJ, Wu P, Senadhira D, Huang N. Mapping QTLs for phosphorus deficiency tolerance in rice (Oryza sativa L.). Theor Appl Genet,1998,97:1361-1369
    104. Niewiadomski P, Knappe S, Geimer S, et al. The Arabidopsis plastidic glucose 6-phosphate/phosphate translocator GPT1 is essential for pollen maturation and embryo sac development. Plant Cell,2005,17:760-775
    105. Olsen KM, Halldorsdottir SS, Stinchcombe JR, et al. Linkage disequilibrium mapping of Arabidopsis CRY2 flowering time alleles. Genetics,2004, 167:1361-1369
    106. Pant BD, Buhtz A, Kerr J, et al. MicroRNA399 is a long distance signal for the regulation of plant phosphate homeostasis. Plant J,2008,53:731-738
    107. Parkin IA, Sharpe AG, Keith DJ, et al. Idetification of the A and C genomes of amphidiploid Brassica napus (oil seedrape). Genome,1995,38:1122-1131.
    108. Parkin IA, Gulden SM, Sharpe AG, et al. Segmental structure of the Brassica napus genome based on comparative analysis with Arabidopsis thaliana. Genetics, 2005,171:765-781
    109. Paszkowski U, Kroken S, Roux C, et al. Rice phosphate transporters include an evolutionarily divergent gene specifically activated in arbuscular mycorrhizal symbiosis. Proc Natl Acad Sci USA,2002,99:13324-13329
    110. Pauline AB, Christie JH, Crispin BT, et al. The Arabidopsis ribonuclease gene RNS1 is tightly controlled in response to phosphate limitation. Plant J,1994,6:673-685
    111. Peek CS, Robson AD, Kuo J. The formation, morphology and anatomy of cluster root of Lupinus albus L. as dependent on soil type and phosphorus supply. Plant Soil, 2003,248:237-246
    112. Pierre Daram, Silvia Brunner, Christine Rausch, et al. Pht2;1 encodes a low-affinity phosphate transporter from Arabidopsis. Plant Cell,1999,11:2153-2166
    113. Piquemal J, Cinquin E, Couton F, et al. Construction of an oilseed rape (Brassica napus L.) genetic map with SSR markers. Theor Appl Genet,2005,111:1514-1523
    114. Poirier Y, Thoma S, Somerville C, et al. A mutant of'Arabidopsis deficient in xylem loading of phosphate. Plant Physiol,1991,97:1087-1093
    115. Pradhan H, Gupta PK, Mukhopadhyay ST, et al. A high-density linkage map in Brassica juncea (Indian mustard) using AFLP and RFLP markers. Theor Appl Genet, 2003,106:607-614
    116. Qiu D, Morgan C, Shi J, et al. A comparative linkage map of oilseed rape and its use for QTL analysis of seed oil and erucic acid content. Theor Appl Genet,2006, 114:67-80
    117. Raghothama KG. Phosphate acqusition. Annu Rev Plant Physiol Plant Mol Biol, 1999,50:665-693
    118. Reiter RS, Coors JG, Sussman MR, et al. Genetic analysis of tolerance to low-phosphorus stress in maize using restriction fragment length polymorphisms. Theor Appl Genet,1991,82:561-568
    119. Reymond M, Svistoonoff S, Loudet O, et al. Identification of QTL controlling root growth response to phosphate starvation in Arabidopsis thaliana. Plant, Cell & Environ,2006,29:115-125
    120. Raboy V, Young KA, Dorsch JA, et al. Genetics and breeding of seed phosphorus and phytic acid. J Plant Physiol,2001,158:489-497
    121. Rubio V, Linhares F, Solano R, et al. A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae. Genes Dev,2001,15:2122-2133.
    122. Salvi S, Tuberosa R, Chiapparino E, et al. Toward positional cloning of Vgtl, a QTL controlling the transition from the vegetative to the reproductive phase in maize. Plant Mol Biol,2002,48:601-613
    123. Sanchez-Calderon L, Lopez-Bucio J, Chacon-Lopez A, et al. Phosphate starvation induces a determinate developmental program in the roots of Arabidopsis thaliana. Plant cell Physiol,2005,46:174-184.
    124. Sanchez-Calderon L, Lopez-Bucio J, Chacon-Lopez A, et al. Characterization of low phosphorus insensitive mutants reveals a crosstalk between low phosphorus-induced determinate root development and the activation of genes involved in the adaptation of Arabidopsis to phosphorus deficiency. Plant Physiol, 2006,140:879-889
    125. Schachtman DP, Shin R. Nutrient sensing and signaling:NPKS. Annu Rev Plant Biol,2007,58:47-69
    126. Schneider KA, Brothers ME, Kelly JD. Marker assisted selection to improve drought resistance in common bean. Crop Sci,1997,37:51-60.
    127. Schranz ME, Lysak MA, Mitchell-Olds T. The ABC's of comparative genomics in the Brassicaceae:building blocks of crucifer genomes. Trends Plant Sci,2006, 11:535-542
    128. Shane MW, Szota C, Lambers H. A root trait accounting for the extreme phosphorus sensitivity of Hakea prostrata (Proteaceae). Plant, Cell &Environ,2004, 27:991-1004
    129. Shane MW, Vos MD, Roock SD, et al.. Shoot P status regulates cluster-root growth and citrate exudation in Lupinus albus grown with a divided root system. Plant, Cell &Environ,2003,26:265-273
    130. Shen J, Rengel Z, Tang C, et al. Role of phosphorus nutrition in development of cluster roots and release of carboxylates in soil-grown Lupinus albus. Plant Soil, 2003,248:199-206
    131. Shi J, Li R, Qiu D, et al. Unraveling the complex trait of crop yield with QTL mapping in Brassica napus. Genetics,2009,182:851-861
    132. Shimizu A, Kato K, Komatsu A, et al. Genetic analysis of root elongation induced by phosphorus deficiency in rice(Oryza sativa L.):fine QTL mapping and multivariate analysis of related traits. Theor Appl Genet,2008,117:987-996
    133. Shimizu A, Yanagihara S, Kawasaki S, et al. Phosphorus deficiency-induced root elongation and its QTL in rice(Oryza sativa L.). Theor Appl Genet,2004, 109:1361-1368
    134. Shin H, Shin HS, Chen RJ, et al. Loss of At4 function impacts phosphate distribution between the roots and the shoots during phosphate starvation. Plant J, 2006,45:712-726.
    135. Shin HS, Dewbreand GR, Harrison MJ. Phosphate transport in Arabidopsis:Pht1;1 and Pht1;4 play a major role in phosphate acquisition from both low-and high-phosphate environments. Plant J,2004,39:629-642
    136. Shoshan H, Sithes L, Mirjana S, et al. Characterization of Arabidopsis acid phosphatase promoter and regulation of acid phosphatase expression. Plamt Physiol, 2000,124:615-626
    137. Solaiman Z, Marschner P, Wang D, et al. Growth, P uptake and rhizosphere properties of wheat and canola genotypes in an alkaline soil with low P availability. Biol Fert Soils,2007,44:143-153
    138. Su J, Xiao Y, Li M, et al. Mapping QTLs for phosphorus-deficiency tolerance at wheat seedling stage. Plant Soil,2006,281:25-36
    139. Su J, Zheng Q, Li H, et al. Detection of QTLs for phosphorus use efficiency in relation to agronomic performance of wheat grown under phosphorus sufficient and limited conditions. Plant Sci,2009,176:824-836
    140. Sun Z, Wang Z, Tu J, et al. An ultradense genetic recombination map for Brassica napus, consisting of 13551 SRAP markers. Theor Appl Genet,2007,114:1305-1317
    141. Suwabe K, Iketani H, Nunome T, et al. Isolation and characterization of microsatellites in Brassica rapa L. Theor Appl Genet,2002,104:1092-1098
    142. Suwabe K, Tsukazaki H, Iketani H, et al. Identification of two loci for resistance to clubroot(Plasmodiophora brassicae Woronin) in Brassica rapa L. Theor Appl Genet,2003,107:997-1002
    143. Suzuki N, Taketa S, Ichii M. Morphological and physiological characteristics of a root-hairless mutant in rice (Oryza sativa L.). Plant Soil,2003,255:9-17
    144. Svistoonoff S, Creff A, Reymond M, et al. Root tip contact with low-phosphate media reprograms plant root architecture. Nat Genet,2007,39:792-796
    145. Tanksley SD, Nelson JC. Advanced backcross QTL analysis:a method for the simultaneous discovery and transfer of valuable QTL from unadapted germplasm into elite breeding lines. Theor Appl Genet,1996,92:191-203
    146. Ticconi CA, Delatorre CA, Lahner B, et al. Arabidopsis pdr2 reveals a phosphate-sensitive checkpoint in root development. Plant J,2004,37:801-814
    147. Tiessen H. Phosphorus in the global environment. In:White PJ and Hammond JP eds,. The Ecophysiology of Plant-Phosphorus Interactions. Netherlands:Springer, 2008,1-7
    148. Uhde-Stone C, Gilbert. G, Johnson JMF, et al. Acclimation of white lupin to phosphorus deficiency involves enhanced expression of genes related to organic acid metabolism. Plant Soil,2003,248:99-116
    149. Valdes-Lopez O, Arenas-Huertero C, Ramirez M, et al. Essential role of MYB transcription factor:PvPHRl and microRNA:PvmiR399 in phosphorus-deficiency signalling in common bean roots. Plant, Cell & Environ,2008,31:1834-1843
    150. Van Ooijen J W. JoinMap 4, software for the calculation of genetic linkage maps in experimental populations. Kyazma BV, Wageningen, Netherlands.2006
    151. Vance CP, Uhde-Stone C, Allan DL. Phosphorus acquisition and use:critical adaptations by plants for securing a nonrenewable resource. New Phytol,2003, 157:423-447
    152. Versaw WK, Harrison MJ. A chloroplast phosphate transporter, PHT2;1, influences allocation of phosphate within the plant and phosphate-starvation responses. Plant Cell,2002,14:1751-1766
    153. Vos P, Hogers R, Bleeker M, et al. AFLP:a new technique for DNA-fingerprinting. Nucl Acids Res,1995,23:4407-4414
    154. Wang L, Liao H, Yan X, et al. Genetic variability for root hair traits as related to phosphorus status in soybean. Plant Soil,2004,261:77-84
    155. Wang SC, Bastern J, Zeng ZB. Windows QTL Cartographer 2.5. Department of Statistics, North Carolina State University, Raleigh, NC.2006
    156. Wang X. Regulatory functions of phospholipase D and phosphatidic acid in plant growth, development, and stress responses. Plant Physiol,2005,139:566-573
    157. Wang Y, Ribot C, Rezzonico E, et al. Structure and expression profile of the Arabidopsis PHO1 gene family indicates a broad role in inorganic phosphate homeostasis. Plant Physiol,2004,135:400-411
    158. Wasaki J, Kojima S, Maruyama H, et al. Localization of acid phosphatase activities in the roots of white lupin plants grown under phosphorus-deficient conditions. Soil Sci Plant Nutr,2008,54:95-102
    159. Watt M, Evans JR. Phosphorus acquisition from soil by white lupin (Lupinus albus L.) and soybean (Glycine max L.), species with contrasting root development. Plant Soil,2003,248:271-283
    160. Weisskopf L, Abou-Mansour E, Fromin N, et al. White lupin has developed a complex strategy to limit microbial degradation of secreted citrate required for phosphate acquisition. Plant, Cell & Environ,2006,29:919-927
    161. Werner JD, Borevitz JO, Warthmann N, et al. Quantitative trait locus mapping and DNA array hybridization identify an FLM deletion as a cause for natural flowering-time variation. Proc Natl Acad Sci USA,2005,102:2460-2465
    162. Williamson LC, Ribrioux SP, Fitter AH, et al. Phosphate availability regulates root system architecture in Arabidopsis. Plant Physiol,2001,126:875-882
    163. Wilson LM, Whitt SR, Ibanez AM, et al. Dissection of maize kernel composition and starch production by candidate gene association. Plant Cell,2004, 16:2719-2733
    164. Wissuwa M, Gamat G, Ismail AM. Is root growth under phosphorus deficiency affected by source or sink limitations? J Exp Bot,2005,56:1943-1950
    165. Wissuwa M, Wegner J, Ae N, et al. Substitution mapping of Pup1:a major QTL increasing phosphorus uptake of rice from a phosphorus-deficient soil. Theor Appl Genet,2002,105:890-897
    166. Wissuwa M, Yano M, Ae N. Mapping of QTLs for phosphorus-deficiency tolerance in rice(Oryza sativa L.). Theor Appl Genet,1998,97:777-783
    167. Wu C, Wei X, Sun HL, et al. Phosphate availability alters lateral root anatomy and root architecture of fraxinus mandshurica rupr seedlings. J Integ Plant Biol,2005, 47:292-301
    168. Xie Y, Yu D. The significance of lateral roots in phosphorus (P) acquisition of water hyacinth. Aquat Bot,2003,75:311-321
    169. Xu FS, Wang YH, Meng JL. Mapping boron efficiency gene(s) in Brassica napus using RFLP and AFLP markers. Plant Breeding,2001,120:319-324
    170. Xue W, Xing Y, Weng X, et al. Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice. Nat Genet,2008,40:761-767
    171. Yadav RS, Tarafdar JC. Influence of organic and inorganic phosphorus supply on the maximumsecretion of acid phosphatase by plants. Biol Fert Soils,2001,34: 140-143
    172. Yan X, Liao H, Beebe SE, et al. QTL mapping of root hair and acid exudation traits and their relationship to phosphorus uptake in common bean. Plant Soil,2004, 265:17-29
    173. Yan X, Wu P, Ling H, et al. Plant nutriomics in China:an overview. Ann Bot (Lond), 2006,98:473-482
    174. Yano M, Katayose Y, Ashikari M, et al. Hdl, a major photoperiod sensitivity quantitative trait locus in rice, is closely related to the Arabidopsis flowering time gene constans. Plant Cell,2000,12:2473-2484
    175. Zakhleniuk OS, Rains CA, Lloyd JC. pho3:a phophorus-deficient mutant of Arabidopsis thalians (L.) Heynh.Planta,2001,212:529-534
    176. Zeng ZB. Precision mapping of quantitative trait loci. Genetics,1994, 136:1457-1468
    177. Zhang D, Cheng H, Geng LY, et al. Detection of quantitative trait loci for phosphorus deficiency tolerance at soybean seedling stage. Euphytica,2009, 167:313-322
    178. Zhang HW, Huang Y, Ye XS, et al. Genotypic differences in phosphorus acquisition and the rhizosphere properties of Brassica napus in response to low phosphorus stress. Plant Soil,2009,320:91-102
    179. Zhang HW, Huang Y, Ye XS, et al. Evaluation of phosphorus efficiency in rapeseed (Brassica napus L.) recombinant inbred lines at seedling stage. Acta Agron Sin, 2008,34(12):2152-2159.
    180. Zhang XW, Jian WU, Zhao JJ. Indentification of QTLs related to bolting in Brassica rarp ssp. Pekinensis. Agr Sci in China.2006,5:265-271
    181. Zhang YJ, Lynch JP, Brown KM. Ethylene and phosphorus availability have interacting yet distinct effects on root hair development. J Exp Bot,2003,54, 391:2351-2361
    182. Zhou J, Jiao FC, Wu ZC, et al. OsPHR2 is involved in phosphate-starvation signaling and excessive phosphate accumulation in shoots of plants. Plant Physiol, 2008,146:1673-1686
    183. Zhu J, Kaeppler SM, Lynch JP. Mapping of QTL controlling root hair length in maize (Zea mays L.) under phosphorus deficiency. Plant Soil,2005a,270:299-310
    184. Zhu J, Kaeppler SM, Lynch JP. Mapping of QTLs for lateral root branching and length in maize (Zea mays L.) under differential phosphorus supply. Theor Appl Genet,2005b,111:688-695
    185. Zhu J, Mickelson SM, Kaeppler SM, et al. Detection of quantitative trait loci for seminal root traits in maize (Zea mays L.) seedlings grown under differential phosphorus levels. Theor Appl Genet,2006,113:1-10
    186. Miura K, Rus A, Sharkhuu A, et al. The Arabidopsis SUMO E3 ligase SIZ1 controls phosphate deficiency responses. Proc Natl Acad Sci USA,2005,102:7760-7766.
    187. Jiang C, Zeng ZB. Multiple trait analysis of genetic map-ping for quantitative trait loci. Genetics,1995 140:1111-1127
    188. Kao CH, Zeng ZB, Teasdale RD. Multiple interval mapping for quantitative trait loci. Genetics,1999,152:1203-1216

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