Development of Genome-wide Simple Sequence Repeat Markers Using Whole-genome Shotgun Sequences of Sorghum (Sorghum bicolor (L.) Moench)

被引:75
作者
Yonemaru, Jun-ichi [1 ]
Ando, Tsuyu [2 ]
Mizubayashi, Tatsumi [2 ]
Kasuga, Shigemitsu [3 ]
Matsumoto, Takashi [1 ]
Yano, Masahiro [1 ]
机构
[1] Natl Inst Agrobiol Sci, Tsukuba, Ibaraki 3058602, Japan
[2] Inst Soc Technoinnovat Agr Forestry & Fisheries, Tsukuba, Ibaraki 3050854, Japan
[3] Shinshu Univ, Fac Agr, Educ & Res Ctr Alpine Field Sci, Minamiminowa, Nagano 3994598, Japan
关键词
sorghum (Sorghum bicolor (L.) Moench); simple sequence repeat (SSR); fragment analysis; genome-wide; LINKAGE-MAP; GENETIC-MAP; SSR-MARKERS; RFLP; RICE; CONSTRUCTION; DIVERSITY; FREQUENCY; BARLEY;
D O I
10.1093/dnares/dsp005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Simple sequence repeat (SSR) markers with a high degree of polymorphism contribute to the molecular dissection of agriculturally important traits in sorghum (Sorghum bicolor (L.) Moench). We designed 5599 non-redundant SSR markers, including regions flanking the SSRs, in whole-genome shotgun sequences of sorghum line ATx623. (AT/TA)(n) repeats constituted 26.1% of all SSRs, followed by (AG/TC)(n) at 20.5%, (AC/TG)(n) at 13.7% and (CG/GC)(n) at 11.8%. The chromosomal locations of 5012 SSR markers were determined by comparing the locations identified by means of electronic PCR with the predicted positions of 34 008 gene loci. Most SSR markers had a similar distribution to the gene loci. Among 970 markers validated by fragment analysis, 67.8% (658 of 970) markers successfully provided PCR amplification in sorghum line BTx623, with a mean polymorphism rate of 45.1% (297 of 658) for all SSR loci in combinations of 11 sorghum lines and one sudangrass (Sorghum sudanense (Piper) Stapf) line. The product of 5012 and 0.678 suggests that similar to 3400 SSR markers could be used to detect SSR polymorphisms and that more than 1500 (45.1% of 3400) markers could reveal SSR polymorphisms in combinations of Sorghum lines.
引用
收藏
页码:187 / 193
页数:7
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