The role of the BRCA1 and BRCA2 gene in the pathogenesis

分子病理学的研究集中在定义基因的变化，这些基因是常见疾病(如癌症和出生缺陷)遗传易感性的基础。目前正在研究的是遗传性乳腺癌和卵巢癌基因BRCA1和BRCA2。这些蛋白质的生物学功能目前尚不清楚。之前，我们发现了哪些蛋白质与BRCA1特异地相互作用。在过去的一年里，我们发现BRCA1对控制其他基因的表达很重要，并且在DNA修复中发挥作用。最近的实验表明，BRCA1似乎有助于识别和消除可能形成肿瘤的细胞。我们现在知道，乳腺癌、卵巢癌和前列腺癌风险的增加与这些基因的遗传变异有关，是因为这些突变的蛋白质无法在DNA修复途径中发挥作用。我们正在使用酵母细胞作为实验模型，以测试在人类中发现的突变的功能后果。我们还开发了一种系统，用于识别与BRCA1相互作用的蛋白质。对BRCA1和BRCA2基因的更多了解将导致改进诊断程序和可能的预防性治疗。

Research in the Molecular Pathogenesis is focused on defining changes in the genes that underlie inherited susceptibilities to common diseases such as cancer and birth defects. Currently under investigation are the inherited breast and ovarian cancer genes, BRCA1 and BRCA2. The biological function of these proteins is currently unknown. Previously we discovered which proteins specifically interact with BRCA1. In the past year we have found that BRCA1 is important for controlling the expression of other genes and is plays a role in DNA repair. Recent experiments has revealed that BRCA1 appears to help in the process of recognizing and eliminating cells that may progress to form tumors. We now know that the increase in breast, ovarian and prostate cancer risk associated with genetic variants in these genes is due to a failure of these mutated proteins to function in the DNA repair pathway. We are using yeast cells as an experimental model to test the functional consequences of mutations found in humans. We have also developed a system for identifying proteins that interact with BRCA1. An increased understanding of the BRCA1 and BRCA2 genes will lead to improved diagnostic procedures and possible preventative therapies.