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微卫星标记在水稻遗传育种中的开发、定位及应用

Microsatellite marker development, mapping and applications in rice genetics and breeding.

作者信息

McCouch S R, Chen X, Panaud O, Temnykh S, Xu Y, Cho Y G, Huang N, Ishii T, Blair M

机构信息

Plant Breeding Department, Cornell University, Ithaca, NY 14853-1901, USA.

出版信息

Plant Mol Biol. 1997 Sep;35(1-2):89-99.

PMID:9291963
Abstract

Microsatellites are simple, tandemly repeated di- to tetra-nucleotide sequence motifs flanked by unique sequences. They are valuable as genetic markers because they are co-dominant, detect high levels of allelic diversity, and are easily and economically assayed by the polymerase chain reaction (PCR). Results from screening a rice genomic library suggest that there are an estimated 5700-10,000 microsatellites in rice, with the relative frequency of different repeats decreasing with increasing size of the motif. A map consisting of 120 microsatellite markers demonstrates that they are well distributed throughout the 12 chromosomes of rice. Five multiple copy primer sequences have been identified that could be mapped to independent chromosomal locations. The current level of genome coverage provided by these simple sequence length polymorphisms (SSLPs) in rice is sufficient to be useful for genotype identification, gene and quantitative trail locus (QTL) analysis, screening of large insert libraries, and marker-assisted selection in breeding. Studies of allelic diversity have documented up to 25 alleles at a single locus in cultivated rice germplasm and provide evidence that amplification in wild relatives of Oryza sativa is generally reliable. The availability of increasing numbers of mapped SSLP markers can be expected to complement existing RFLP and AFLP maps, increasing the power and resolution of genome analysis in rice.

摘要

微卫星是由独特序列侧翼的简单串联重复二至四核苷酸序列基序。它们作为遗传标记很有价值,因为它们是共显性的,能检测到高水平的等位基因多样性,并且通过聚合酶链反应(PCR)易于且经济地进行检测。对水稻基因组文库进行筛选的结果表明,水稻中估计有5700 - 10000个微卫星,不同重复序列的相对频率随着基序大小的增加而降低。由120个微卫星标记组成的图谱表明,它们在水稻的12条染色体上分布良好。已鉴定出五个多拷贝引物序列,它们可被定位到独立的染色体位置。水稻中这些简单序列长度多态性(SSLP)目前的基因组覆盖水平足以用于基因型鉴定、基因和数量性状位点(QTL)分析、大插入文库的筛选以及育种中的标记辅助选择。等位基因多样性研究记录了栽培稻种质中单个位点上多达25个等位基因,并提供证据表明在栽培稻的野生近缘种中扩增通常是可靠的。预计越来越多已定位的SSLP标记的可用性将补充现有的RFLP和AFLP图谱,提高水稻基因组分析的能力和分辨率。

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