柑橘属植物微卫星分析

JIANG Dong, ZHONG Guang-Yan, HONG Qi-Bing
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引用次数: 41

摘要

对甜橙(Citrus sinensis osbeck)、三叶橙(Poncirus trifoliata Raf.)等柑橘品种和栽培品种的EST单基因序列进行了简单序列重复序列(SSRs)分析。共检索到23.29 Mb的37 802条柑橘单基因序列,鉴定出8 218条SSRs。其中单核苷酸SSRs 4 913例(59.8%),二核苷酸SSRs 1 419例(17.3%),三核苷酸SSRs 1 709例(20.8%),四核苷酸SSRs 114例(1.39%),五核苷酸SSRs 23例(0.28%),六核苷酸SSRs 40例(0.49%)。估计ssr的频率约为1/2.8 kb,可推断为4.6个单基因中含有1个ssr。根据序列重复数的不同,SSR的最大长度在40 ~ 105 bp之间。SSRs的总平均长度为20.9 bp。甜橙和三叶橙不同SSR类型(二核苷酸、三核苷酸、四核苷酸和五核苷酸重复)的频率非常相似。甜橙和三叶橙中单核苷酸重复序列最多,其次是三聚体重复序列。A/T、AG、AT、AAG、AAAT、AAAG、AAAG、AAAT、AAAT、AAAAG、AAAAG、AAAAT等富含腺嘌呤的重复序列在单-、二-、三-、四-和五- SSRs中占主导地位,而C/G、CG、CCG重复序列较少。设计了25对EST-SSR位点侧翼引物,对甜橙和三叶橙等6个柑桔品种的EST-SSR多态性进行了检测。25对引物的PCR结果显示,6个柑橘品种存在多态性,表明柑橘EST数据库可以有效地用于开发基因源性SSR标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of Microsatellites in Citrus Unigenes

Simple sequence repeats (SSRs) were investigated in the unigene sequences from expressed sequence tags (EST) of sweet orange (Citrus sinensis osbeck), trifoliate orange (Poncirus trifoliata Raf.) and other citrus species and cultivars. A total of 37 802 citrus unigene sequences corresponding to 23.29 Mb were searched, resulting in the identification of 8 218 SSRs. Among them there were 4 913 (59.8%) mono-, 1 419 (17.3%) di-, 1 709 (20.8%) tri-, 114 (1.39%) tetra-, 23 (0.28%) penta- and 40 (0.49%) hexa-nucleotide SSRs. The estimated frequency of SSRs was approximately 1/2.8 kb, which could be extrapolated to 1 SSR-containing unigene in 4.6 unigenes. The maximum length of the SSR ranged from 40 to 105 bp depending on the repeating numbers of the motif in the SSR. The overall average length of SSRs was 20.9 bp. The frequencies of different SSR types (di-, tri-, tetra-, and penta-nucleotide repeats) were very similar between sweet orange and trifoliate orange. The mononucelotide repeats appeared to be the most abundant SSRs within sweet orange and trifoliate orange, followed by trimeric repeats. The adenine rich repeats such as A/T, AG, AT, AAG, AAAT, AAAG, AAAT, AAAAG, AAAAT etc. were predominant in each type of SSRs (mono-, di-, tri-, tetra-, and penta-), whereas the C/G, CG, CCG repeats were less abundant. Twenty-five primer pairs flanking EST-SSR loci were designed to detect the possible polymorphism of six citrus cultivars including sweet orange and trifoliate orange. The PCR result with all these 25 primer pairs revealed the existence of polymorphism within six citrus cultivars confirming that citrus EST database could be efficiently exploited for the development of gene-derived SSR markers.

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