Key Laboratory of Horticultural Plant Biology (MOE), National Center of Citrus Breeding, Huazhong Agricultural University, 430070, Wuhan, People's Republic of China.
Mol Biol Rep. 2012 May;39(5):5373-86. doi: 10.1007/s11033-011-1338-5. Epub 2011 Dec 15.
The aim of this study was to develop a large set of microsatellite markers based on publicly available BAC-end sequences (BESs), and to evaluate their transferability, discriminating capacity of genotypes and mapping ability in Citrus. A set of 1,281 simple sequence repeat (SSR) markers were developed from the 46,339 Citrus clementina BAC-end sequences (BES), of them 20.67% contained SSR longer than 20 bp, corresponding to roughly one perfect SSR per 2.04 kb. The most abundant motifs were di-nucleotide (16.82%) repeats. Among all repeat motifs (TA/AT)n is the most abundant (8.38%), followed by (AG/CT)n (4.51%). Most of the BES-SSR are located in the non-coding region, but 1.3% of BES-SSRs were found to be associated with transposable element (TE). A total of 400 novel SSR primer pairs were synthesized and their transferability and polymorphism tested on a set of 16 Citrus and Citrus relative's species. Among these 333 (83.25%) were successfully amplified and 260 (65.00%) showed cross-species transferability with Poncirus trifoliata and Fortunella sp. These cross-species transferable markers could be useful for cultivar identification, for genomic study of Citrus, Poncirus and Fortunella sp. Utility of the developed SSR marker was demonstrated by identifying a set of 118 markers each for construction of linkage map of Citrus reticulata and Poncirus trifoliata. Genetic diversity and phylogenetic relationship among 40 Citrus and its related species were conducted with the aid of 25 randomly selected SSR primer pairs and results revealed that citrus genomic SSRs are superior to genic SSR for genetic diversity and germplasm characterization of Citrus spp.
本研究旨在基于公开的 BAC 末端序列(BES)开发一套大量的微卫星标记,并评估其在柑橘中的转移能力、基因型的区分能力和作图能力。从 46339 个柑橘克莱门汀 BAC 末端序列(BES)中开发了一套 1281 个简单序列重复(SSR)标记,其中 20.67%的序列含有长度超过 20 bp 的 SSR,大致每 2.04 kb 就有一个完整的 SSR。最丰富的基序是二核苷酸(16.82%)重复。在所有重复基序中,(TA/AT)n 是最丰富的(8.38%),其次是(AG/CT)n(4.51%)。大多数 BES-SSR 位于非编码区,但有 1.3%的 BES-SSR 与转座元件(TE)相关。共合成了 400 对新的 SSR 引物,并在一组 16 个柑橘及其亲缘种上测试了其转移能力和多态性。其中 333 对(83.25%)成功扩增,260 对(65.00%)与枳和金桔具有跨物种转移性。这些跨物种可转移性标记物可用于品种鉴定、柑橘、枳和金桔的基因组研究。通过构建柑橘和枳的连锁图谱,证明了所开发的 SSR 标记的实用性。利用 25 对随机选择的 SSR 引物对 40 个柑橘及其相关种进行了遗传多样性和系统发育关系分析,结果表明,柑橘基因组 SSR 比基因 SSR 更适合柑橘属的遗传多样性和种质特征分析。