Chen R, Wang B, Zhang Y, Liu W, Zhang J, Lao W
Institute of Biophysics, Chinese Academy of Sciences, Beijing.
Chin J Biotechnol. 1992;8(3):159-69.
We have isolated a clone from a EMBL3 constructed bovine genomic library using a PCR-generated DNA fragment as a probe covering-660bp to + 158 bp of boving alpha-sl casein gene. The results obtained from hybridization assay, restriction endonucleases map and partial DNA sequence analysis indicated that the cloned fragment spanned 5.7kb of the first part of the gene and 8.0 kb of its upstream flanking region. Some divergent restriction endonuclease recognition sites and a few mutations and deletions were found in exons, introns and 5'-flanking region of the gene we cloned when compared with the PCR-generated fragment and those which had been published [6,10]. All the deletions occurred at repeat sequences.
我们使用一个PCR扩增的DNA片段作为探针,从构建的EMBL3牛基因组文库中分离出一个克隆,该探针覆盖牛αs1酪蛋白基因的-660bp至+158bp区域。杂交分析、限制性内切酶图谱分析和部分DNA序列分析结果表明,克隆片段跨越该基因第一部分的5.7kb及其上游侧翼区域的8.0kb。与PCR扩增片段及已发表的序列[6,10]相比,我们克隆的基因在外显子、内含子和5'侧翼区域发现了一些不同的限制性内切酶识别位点、一些突变和缺失。所有缺失均发生在重复序列处。