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小鼠有丝分裂和减数分裂细胞中Brca1和Brca2的表达模式。

Brca1 and Brca2 expression patterns in mitotic and meiotic cells of mice.

作者信息

Blackshear P E, Goldsworthy S M, Foley J F, McAllister K A, Bennett L M, Collins N K, Bunch D O, Brown P, Wiseman R W, Davis B J

机构信息

National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.

出版信息

Oncogene. 1998 Jan 8;16(1):61-8. doi: 10.1038/sj.onc.1201506.

Abstract

The mouse homologues of the breast cancer susceptibility genes, Brca1 and Brca2, are expressed in a cell cycle-dependent fashion in vitro and appear to be regulated by similar or overlapping pathways. Therefore, we compared the non isotopic in situ hybridization expression patterns of Brca1 and Brca2 mRNA in vivo in mitotic and meiotic cells during mouse embryogenesis, mammary gland development, and in adult tissues including testes, ovaries, and hormonally altered ovaries. Brca1 and Brca2 are expressed concordantly in proliferating cells of embryos, and the mammary gland undergoing morphogenesis and in most adult tissues. The expression pattern of Brca1 and Brca2 correlates with the localization of proliferating cell nuclear antigen, an indicator of proliferative activity. In the ovary, Brca1 and Brca2 exhibited a comparable hormone-independent pattern of expression in oocytes, granulosa cells and thecal cells of developing follicles. In the testes, Brca1 and Brca2 were expressed in mitotic spermatogonia and early meiotic prophase spermatocytes. Northern analyses of prepubertal mouse testes revealed that the time course of Brca2 expression was delayed in spermatogonia relative to Brca1. Thus, while Brca1 and Brca2 share concordant cell-specific patterns of expression in most proliferating tissues, these observations suggest that they may have distinct roles during meiosis.

摘要

乳腺癌易感基因Brca1和Brca2的小鼠同源物在体外以细胞周期依赖性方式表达,并且似乎受相似或重叠的信号通路调控。因此,我们比较了Brca1和Brca2 mRNA在小鼠胚胎发育、乳腺发育过程中以及在包括睾丸、卵巢和激素处理后的卵巢在内的成年组织的有丝分裂和减数分裂细胞中的非同位素原位杂交表达模式。Brca1和Brca2在胚胎的增殖细胞、正在进行形态发生的乳腺以及大多数成年组织中协同表达。Brca1和Brca2的表达模式与增殖细胞核抗原(一种增殖活性指标)的定位相关。在卵巢中,Brca1和Brca2在发育卵泡的卵母细胞、颗粒细胞和卵泡膜细胞中呈现出类似的激素非依赖性表达模式。在睾丸中,Brca1和Brca2在有丝分裂的精原细胞和减数分裂前期早期的精母细胞中表达。对青春期前小鼠睾丸的Northern分析显示,相对于Brca1,Brca2在精原细胞中的表达时间进程延迟。因此,虽然Brca1和Brca2在大多数增殖组织中具有一致的细胞特异性表达模式,但这些观察结果表明它们在减数分裂过程中可能具有不同的作用。

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