首页> 美国卫生研究院文献>Comparative Cytogenetics >Genomic in situ hybridization in interspecific hybrids of scallops (Bivalvia Pectinidae) and localization of the satellite DNA Cf303 and the vertebrate telomeric sequences (TTAGGG)n on chromosomes of scallop Chlamysfarreri (Jones Preston 1904)
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Genomic in situ hybridization in interspecific hybrids of scallops (Bivalvia Pectinidae) and localization of the satellite DNA Cf303 and the vertebrate telomeric sequences (TTAGGG)n on chromosomes of scallop Chlamysfarreri (Jones Preston 1904)

机译:扇贝(BivalviaPectinidae)种间杂种的基因组原位杂交和卫星DNA Cf303的定位以及扇贝衣原体染色体上的脊椎动物端粒序列(TTAGGG)nfarreri(琼斯和普雷斯顿1904年)

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摘要

Mitotic chromosome preparations of the interspecific hybrids Chlamys farreri (Jones & Preston, 1904) × Patinopecten yessoensis (Jay, 1857), C. farreri × Argopecten irradians (Lamarck, 1819) and C. farreri × Mimachlamys nobilis (Reeve, 1852) were used to compare two different scallop genomes in a single slide. Although genomic in situ hybridization (GISH) using genomic DNA from each scallop species as probe painted mitotic chromosomes of the interspecific hybrids, the painting results were not uniform; instead it showed species-specific distribution patterns of fluorescent signals among the chromosomes. The most prominent GISH-bands were mainly located at centromeric or telomeric regions of scallop chromosomes. In order to illustrate the sequence constitution of the GISH-bands, the satellite Cf303 sequences of C. farreri and the vertebrate telomeric (TTAGGG)n sequences were used to map mitotic chromosomes of C. farreri by fluorescence in situ hybridization (FISH). The results indicated that the GISH-banding pattern presented by the chromosomes of C. farreri is mainly due to the distribution of the satellite Cf303 DNA, therefore suggesting that the GISH-banding patterns found in the other three scallops could also be the result of the chromosomal distribution of other species-specific satellite DNAs.
机译:种间杂种Chlamys farreri(Jones&Preston,1904)×Patinopecten yessoensis(Jay,1857),C。farreri×Argopecten irradians(Lamarck,1819)和 C。 farreri × < em class =“ genus”> Mimachlamys nobilis (里夫,1852年)被用于在一张幻灯片中比较两个扇贝基因组。尽管使用每种扇贝物种的基因组DNA作为探针绘制了种间杂种的有丝分裂染色体的基因组原位杂交(GISH),但绘制结果并不均匀。相反,它显示了染色体之间荧光信号的特定物种分布模式。最突出的GISH带主要位于扇贝染色体的着丝粒或端粒区域。为了说明GISH频段的序列构成,使用了 C的卫星 Cf303 序列。 em> farreri 和脊椎动物端粒(TTAGGG)n序列用于定位 C。 farreri 通过荧光原位杂交(鱼)。结果表明, C。 farreri的染色体呈现的GISH带模式 主要是由于卫星 Cf303 DNA的分布,因此表明在其他三个扇贝中发现的GISH条带模式也可能是其结果其他物种特有的卫星DNA的染色体分布图。

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