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染色体显微切割与DOP-PCR结合对赤麂Sry基因克隆、测序及初步定位
Cloning, Sequencing and Chromosome Location of Sry Gene of Muntjak munticus vaginalis by DOP-PCR and Microdissection
【摘要】 应用显微切割技术获得赤麂1号、Y1、Y2染色体,通过DOP-PCR增加模板DNA拷贝数,然后用人的性别决定基因(Sex-determining Region of the Chromosome Y, SRY)中HMG框内设计1对引物,对DOP-PCR产物进行扩增。在雄性赤麂Y2染色体DOP-PCR产物中扩增出与人SRY基因同源的Sry基因片段,克隆、测序,首次在分子水平上证明赤麂Y2染色体是真正的Y染色体,同时对赤麂Sry基因进行了初步定位。
【Abstract】 We isolated 1, Y1, Y2 chromosomes of the male M.m vaginalis by microdissection and amplified the DNA copies by DOP-PCR. Using the DOP-PCR products of 1, Y1, Y2 chromosomes of M.m vaginalis as template respectively and the primers designed within human SRY HMG box, the Sry gene of the male M.m vaginalis was amplified, and it was cloned and sequenced. It is proved that Y2 is the real sex chromosome in the male M.m vaginalis at molecular level for the first time, and Sry was localized on Y2 chromosome.
【Key words】 microdissection; DOP-PCR; Sry gene; M.m. vaginalis; sex chromosome; chromosome location;
- 【文献出处】 遗传学报 ,Acta Genetica Sinica , 编辑部邮箱 ,2001年04期
- 【分类号】Q953
- 【被引频次】19
- 【下载频次】152