巴西橡胶树EST-SSR标记的系统鉴定及引物筛选

IF 1.3 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of Nucleic Acids Pub Date : 2017-01-01 Epub Date: 2017-01-23 DOI:10.1155/2017/6590902
Benjun Hou, Suping Feng, Yaoting Wu
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引用次数: 13

摘要

本研究旨在利用SSR (Simple sequence Repeat)技术对巴西橡胶树表达序列标签(EST)信息进行系统鉴定和初步验证,为进一步开发SSR分子标记提供依据。确定橡胶树EST剪接序列的一般SSR特征并开发引物,为橡胶树资源的多样性分析和品种鉴定奠定了基础。在EST剪接序列中鉴定出1134个SSR位点,分布在840个Unigene中。SSR位点的发生率为23.9%,EST-SSR平均分布距离为2.59 kb。以单核苷酸重复基序为主,占38.89%,二核苷酸重复基序占36.95%,三核苷酸重复基序占18.17%;其他图案的比例仅为5.99%。单核苷酸、二核苷酸和三核苷酸的优势重复基序分别为A/T、AG/CT和AAG/CTT。共设计引物739对,共1134个SSR位点。对Hevea热炎5-11、热炎87-6-47和PR107进行PCR扩增,筛选出能扩增多态性条带的引物180对。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Systemic Identification of <i>Hevea brasiliensis</i> EST-SSR Markers and Primer Screening.

Systemic Identification of <i>Hevea brasiliensis</i> EST-SSR Markers and Primer Screening.

Systemic Identification of <i>Hevea brasiliensis</i> EST-SSR Markers and Primer Screening.

Systemic Identification of Hevea brasiliensis EST-SSR Markers and Primer Screening.

This research aimed to systematically identify and preliminarily validate the Hevea brasiliensis expressed sequence tag (EST) information using Simple Sequence Repeat (SSR) and provide evidence for further development of SSR molecular marker. The definition of general SSR features of Hevea EST splicing sequences and development of SSR primers founded the basis of diversity analysis and variety identification for Hevea tree resource. 1134 SSR loci were identified in the EST splicing sequence and distributed in 840 Unigene. The occurrence rate of SSR loci was 23.9%, and the average distribution distance of EST-SSR was 2.59 kb. The major repeat type was mononucleotide repeat motif, which accounted for 38.89%, while the corresponding value was 36.95% for dinucleotide repeat motif and 18.17% for trinucleotide repeat motif; the proportion of other motifs was only 5.99%. The superior repeat motifs for mononucleotide, dinucleotide, and trinucleotide were A/T, AG/CT, and AAG/CTT, respectively. 739 pair of primers were designed for 1134 SSR loci. PCR amplification was performed on Hevea Reyan5-11, Reyan87-6-47, and PR107, and 180 pairs of primers were selected which were able to amplify polymorphism bands.

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来源期刊
Journal of Nucleic Acids
Journal of Nucleic Acids BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.10
自引率
21.70%
发文量
5
审稿时长
12 weeks
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