Jensen R A, Thompson M E, Jetton T L, Szabo C I, van der Meer R, Helou B, Tronick S R, Page D L, King M C, Holt J T
Department of Pathology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-5310, USA.
Nat Genet. 1996 Mar;12(3):303-8. doi: 10.1038/ng0396-303.
Germline mutations in BRCA1 are responsible for most cases of inherited breast and ovarian cancer. However, the function of the BRCA1 protein has remained elusive. We now show that BRCA1 encodes a 190-kD protein with sequence homology and biochemical analogy to the granin protein family. Interestingly, BRCA2 also includes a motif similar to the granin consensus at the C terminus of the protein. Both BRCA1 and the granins localize to secretory vesicles, are secreted by a regulated pathway, are post-translationally glycosylated and are responsive to hormones. As a regulated secretory protein, BRCA1 appears to function by a mechanism not previously described for tumour suppressor gene products.
BRCA1基因的种系突变是大多数遗传性乳腺癌和卵巢癌的病因。然而,BRCA1蛋白的功能仍然难以捉摸。我们现在发现,BRCA1编码一种190-kD的蛋白,该蛋白与嗜铬粒蛋白家族在序列上具有同源性,在生化特性上具有相似性。有趣的是,BRCA2在其蛋白的C末端也包含一个与嗜铬粒蛋白共有基序相似的基序。BRCA1和嗜铬粒蛋白均定位于分泌囊泡,通过调节途径分泌,进行翻译后糖基化修饰,并对激素产生反应。作为一种受调节的分泌蛋白,BRCA1似乎通过一种先前未描述的肿瘤抑制基因产物机制发挥作用。