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Chromosomal mapping of tandem repeats in the Yesso Scallop Patinopectenyessoensis (Jay 1857) utilizing fluorescence in situ hybridization

机译:斑节扇贝Yesso扇贝中串联重复序列的染色体作图yessoensis(Jay1857)利用荧光原位杂交

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摘要

Construction of cytogenetic maps can provide important information for chromosome identification, chromosome evolution and genomic research. However, it hasn’t been conducted in many scallop species yet. In the present study, we attempted to map 12 fosmid clones containing tandem repeats by fluorescence in situ hybridization (FISH) in the Yesso scallop Patinopecten yessoensis (Jay, 1857). The results showed 6 fosmid clones were successfully mapped and distributed in 6 different pairs of chromosomes. Three clones were respectively assigned to a pair of metacentric chromosomes, a pair of submetacentric chromosomes and a pair of telocentric chromosomes and the remaining 3 clones showed their loci on three different pairs of subtelocentric chromosomes by co-hybridization. In summary, totally 8 pairs of chromosomes of the Yesso scallop were identified by 6 fosmid clones and two rDNA probes. Furthermore, 6 tandem repeats of 5 clones were sequenced and could be developed as chromosome specific markers for the Yesso scallop. The successful localization of fosmid clones will undoubtedly facilitate the integration of linkage groups with cytogenetic map and genomic research for the Yesso scallop.
机译:细胞遗传图谱的构建可以为染色体鉴定,染色体进化和基因组研究提供重要信息。但是,尚未在许多扇贝物种中进行过。在本研究中,我们试图通过Yesso扇贝Patinopecten yessoensis的荧光原位杂交(FISH)绘制12个包含串联重复序列的fosmid克隆(Jay,1857)。结果表明,成功克隆了6个fosmid克隆并将其分布在6对不同的染色体中。将三个克隆分别分配给一对亚中心染色体,一对亚中心染色体和一对端中心染色体,其余三个克隆通过共杂交在三对不同的亚中心染色体上显示了它们的基因座。总之,通过6个fosmid克隆和2个rDNA探针鉴定出总共8对Yesso扇贝染色体。此外,对5个克隆的6个串联重复序列进行了测序,可以开发为Yesso扇贝的染色体特异性标记。 fosmid克隆的成功定位无疑将促进连接基团与Yesso扇贝的细胞遗传图谱和基因组研究的整合。

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