Bennett L M, Haugen-Strano A, Cochran C, Brownlee H A, Fiedorek F T, Wiseman R W
Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.
Genomics. 1995 Oct 10;29(3):576-81. doi: 10.1006/geno.1995.9963.
The BRCA1 gene is in large part responsible for hereditary human breast and ovarian cancer. Here we report the isolation of the murine Brca1 homologue cDNA clones. In addition, we identified genomic P1 clones that contain most, if not all, of the mouse Brca1 locus. DNA sequence analysis revealed that the mouse and human coding regions are 75% identical at the nucleotide level while the predicted amino acid identity is only 58%. A DNA sequence variant in the Brca1 locus was identified and used to map this gene on a (Mus m. musculus Czech II x C57BL/KsJ)F1 x C57BL/KsJ intersubspecific backcross to distal mouse chromosome 11. The mapping of this gene to a region highly syntenic with human chromosome 17, coupled with Southern and Northern analyses, confirms that we isolated the murine Brca1 homologue rather than a related RING finger gene. The isolation of the mouse Brca1 homologue will facilitate the creation of mouse models for germline BRCA1 defects.
BRCA1基因在很大程度上导致人类遗传性乳腺癌和卵巢癌。在此我们报告小鼠Brca1同源cDNA克隆的分离。此外,我们鉴定出了基因组P1克隆,这些克隆包含了大部分(如果不是全部的话)小鼠Brca1基因座。DNA序列分析显示,小鼠和人类的编码区在核苷酸水平上有75%的同一性,而预测的氨基酸同一性仅为58%。在Brca1基因座中鉴定出一个DNA序列变异,并利用它将该基因定位在(小家鼠捷克II品系×C57BL/KsJ品系)F1与C57BL/KsJ品系的种间回交后代上,定位于小鼠远端11号染色体。该基因定位于与人类17号染色体高度同线的区域,再结合Southern和Northern分析,证实我们分离出的是小鼠Brca1同源物,而非相关的环指基因。小鼠Brca1同源物的分离将有助于创建生殖系BRCA1缺陷的小鼠模型。