Zhai W, Chen X, Wu D, Xu J, Gao Y, Zhu L
Institute of Genetics, Chinese Academy of Sciences, Beijing.
Chin J Biotechnol. 1993;9(2):79-84.
Based on the highly conserved region of human, rabbit and mouse SRY (sex-determining region Y) sequences, primers were designed for the amplification of the unknown homologous sequence of cattle by polymerase chain reaction (PCR). A 200-bp male-specific amplifying fragment was obtained. The fragment shares high homology with the known SRY gene. By using the cloned fragment as a probe to hybridize to the Southern blot of HindIII-digested cattle genomic DNA, a 1.7-kb male-specific fragment was detected, which is considered to contain the 200-bp fragment. When the same pair of primers was used in amplification of human and goat DNA samples, the 200-bp male-specific fragment could be detected.
根据人、兔和小鼠SRY(Y染色体性别决定区)序列的高度保守区域,设计引物,通过聚合酶链反应(PCR)扩增牛的未知同源序列。获得了一个200bp的雄性特异性扩增片段。该片段与已知的SRY基因具有高度同源性。以克隆的片段为探针,与经HindIII消化的牛基因组DNA的Southern杂交印迹杂交,检测到一个1.7kb的雄性特异性片段,该片段被认为包含200bp的片段。当使用同一对引物扩增人及山羊DNA样本时,可检测到200bp的雄性特异性片段。