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从小麦EST序列中开发的101个新的微卫星位点(EST-SSR)。

One hundred and one new microsatellite loci derived from ESTs (EST-SSRs) in bread wheat.

作者信息

Gao L F, Jing R L, Huo N X, Li Y, Li X P, Zhou R H, Chang X P, Tang J F, Ma Z Y, Jia J Z

机构信息

Key Laboratory of Crop Germplasm and Biotechnology, Ministry of Agriculture, Institute of Crop Germplasm Resources, Chinese Academy of Agricultural Sciences, 100081 Beijing, China.

出版信息

Theor Appl Genet. 2004 May;108(7):1392-400. doi: 10.1007/s00122-003-1554-z. Epub 2004 Feb 14.

Abstract

Four hundred and seventy-eight microsatellite markers derived from expressed sequence tags (EST-SSRs) were screened among three mapping populations (W-7984xOpata 85, WOpop; LumaixHanxuan, LHpop; WenmaixShanhongmai, WSpop). The number of polymorphic EST-SSR primer pairs found in WOpop, LHpop and WSpop was 92, 58 and 29 respectively. A total of 101 EST-SSR loci amplified from 88 primer sets were distributed over the 20 chromosomes of the reference maps (no markers were located on chromosome 4B). These 101 mapped EST-SSR markers add to the existing 450 microsatellite loci previously mapped in bread wheat. Seventy-four of the 101 loci showed significant similarities to known genes, including 24 genes involved in metabolism, 4 in cellular structures, 9 in stress resistance, 12 in transcription, 2 in development, 2 transporters and 21 storage proteins. Besides gliadin and glutenin, most of the 53 genes with putative functions were mapped for the first time by EST-SSR markers in bread wheat. Sequence alignment of the mapped wheat EST-SSR loci allowed tentative assignment of functionality to the other members of grasses family. Colinearity combined with homology information offers an attractive approach to comparative genomics.

摘要

在三个作图群体(W-7984×Opata 85,WOpop;鲁麦14×邯6172,LHpop;温麦6×陕253,WSpop)中筛选了478个来源于表达序列标签的微卫星标记(EST-SSR)。在WOpop、LHpop和WSpop中发现的多态性EST-SSR引物对数量分别为92、58和29。从88个引物组扩增得到的101个EST-SSR位点分布在参考图谱的20条染色体上(4B染色体上没有标记)。这101个定位的EST-SSR标记增加到了先前在普通小麦中定位的450个微卫星位点中。101个位点中的74个与已知基因有显著相似性,包括24个参与代谢的基因、4个参与细胞结构的基因、9个参与抗逆性的基因、12个参与转录的基因、2个参与发育的基因、2个转运蛋白基因和21个贮藏蛋白基因。除了醇溶蛋白和谷蛋白外,53个具有推定功能的基因中的大多数是首次通过EST-SSR标记在普通小麦中定位的。对定位的小麦EST-SSR位点进行序列比对,有助于初步确定禾本科其他成员的功能。共线性结合同源性信息为比较基因组学提供了一种有吸引力的方法。

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