生物
遗传学
限制性片段长度多态性
水稻
回交
人口
cDNA文库
互补DNA
基因组
普通大麦
基因定位
基因组文库
限制地点
限制性酶
聚合酶链反应
植物
基因
禾本科
染色体
肽序列
人口学
社会学
作者
M A Causse,T. M. Fulton,Y G Cho,S Ahn,Julapark Chunwongse,Kai Wu,Jinhua Xiao,Zheping Yu,Pamela C. Ronald,Sandra E. Harrington
出处
期刊:Genetics
[Oxford University Press]
日期:1994-12-01
卷期号:138 (4): 1251-1274
被引量:849
标识
DOI:10.1093/genetics/138.4.1251
摘要
Abstract A molecular map has been constructed for the rice genome comprised of 726 markers (mainly restriction fragment length polymorphisms; RFLPs). The mapping population was derived from a backcross between cultivated rice, Oryza sativa, and its wild African relative, Oryza longistaminata. The very high level of polymorphism between these species, combined with the use of polymerase chain reaction-amplified cDNA libraries, contributed to mapping efficiency. A subset of the probes used in this study was previously used to construct an RFLP map derived from an inter subspecific cross, providing a basis for comparison of the two maps and of the relative mapping efficiencies in the two crosses. In addition to the previously described PstI genomic rice library, three cDNA libraries from rice (Oryza), oat (Avena) and barley (Hordeum) were used in this mapping project. Levels of polymorphism detected by each and the frequency of identifying heterologous sequences for use in rice mapping are discussed. Though strong reproductive barriers isolate O. sativa from O. longistaminata, the percentage of markers showing distorted segregation in this backcross population was not significantly different than that observed in an intraspecific F2 population previously used for mapping. The map contains 1491 cM with an average interval size of 4.0 cM on the framework map, and 2.0 cM overall. A total of 238 markers from the previously described PstI genomic rice library, 250 markers from a cDNA library of rice (Oryza), 112 cDNA markers from oat (Avena), and 20 cDNA markers from a barley (Hordeum) library, two genomic clones from maize (Zea), 11 microsatellite markers, three telomere markers, eleven isozymes, 26 cloned genes, six RAPD, and 47 mutant phenotypes were used in this mapping project. Applications of a molecular map for plant improvement are discussed.
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