《基于“酥梨”芽转录组的简单序列重复(SSR)标记开发 Development of genic SSR markers from transcriptome sequencing of pear buds》.pdfVIP
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《基于“酥梨”芽转录组的简单序列重复(SSR)标记开发 Development of genic SSR markers from transcriptome sequencing of pear buds》.pdf
Yue et al. / J Zhejiang Univ-Sci B (Biomed Biotechnol) 2014 15(4):303-312 303
Journal of Zhejiang University-SCIENCE B (Biomedicine Biotechnology)
ISSN 1673-1581 (Print); ISSN 1862-1783 (Online)
/jzus;
E-mail: jzus@
Development of genic SSR markers from
*#
transcriptome sequencing of pear buds
1 1,2 1 †‡1 †‡1
Xiao-yan YUE , Guo-qin LIU , Yu ZONG , Yuan-wen TENG , Dan-ying CAI
1
( State Agricultural Ministry Key Laboratory of Horticultural Plant Growth, Development Quality Improvement,
Department of Horticulture, Zhejiang University, Hangzhou 310058, China)
(2 College of Agriculture, Guizhou University, Guiyang 550025, China)
†E-mail: ywteng@; dycai@
Received Sept. 6, 2013; Revision accepted Dec. 3, 2013; Crosschecked Mar. 13, 2014
Abstract: A total of 8375 genic simple sequence repeat (SSR) loci were discovered from a unigene set assembled
from 116 282 transcriptomic unigenes in this study. Dinucleotide repeat motifs were the most common with a frequency
of 65.11%, followed by trinucleotide (32.81%). A total of 4100 primer pairs were designed from the SSR loci. Of these,
343 primer pairs (repeat length ≥15 bp) were synthesized with an M13 tail and tested for stable amplification and
polymorphism in four Pyrus accessions. After the preliminary test, 104 polymorphic genic SSR markers were devel-
oped; dinucleotide and trinucleotide rep
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