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核输入负调控因子BRCA1结合蛋白2的相互作用组

Interactome of the negative regulator of nuclear import BRCA1-binding protein 2.

作者信息

Fatima Shadma, Wagstaff Kylie M, Loveland Kate L, Jans David A

机构信息

Department.of Biochemistry &Molecular Biology Monash University, Clayton, Victoria, Australia.

Department of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.

出版信息

Sci Rep. 2015 Mar 30;5:9459. doi: 10.1038/srep09459.

Abstract

Although the negative regulator of nuclear import (NRNI) BRCA1 binding protein 2 (BRAP2) is highly expressed in testis, its role is largely unknown. Here we address this question by documenting the BRAP2 interactome from human testis, using the yeast 2-hybrid system to identify BRAP2-interacting proteins with roles in diverse cellular processes, including regulation of the actin cytoskeleton, ubiquitinylation, cell cycle/apoptosis and transcription. Interaction with BRAP2 in adult mouse testis with three of these, PH domain and leucine rich repeat protein phosphatase 1 (PHLPP1), A-Kinase anchor protein (AKAP3) and DNA methyl transferase 1 (DNMT1), was confirmed by coimmunoprecipitation assays. BRAP2's ability to inhibit PHLPP1 and DNMT1 nuclear localisation was also confirmed by quantitative confocal microscopy. Importantly, the physiological relevance thereof was implied by the cytoplasmic localisation of PHLPP1, AKAP3 and DNMT1 in pachytene spermatocytes/round spermatids where BRAP2 is present at high levels, and nuclear localisation of PHLPP1 and DNMT1 in spermatogonia concomitant with lower levels of BRAP2. Interestingly, BRAP2 was also present in murine spermatozoa, in part colocalised with AKAP3. Together the results indicate for the first time that BRAP2 may play an important NRNI role in germ cells of the testis, with an additional, scaffold/structural role in mature spermatozoa.

摘要

尽管核输入负调节因子(NRNI)BRCA1结合蛋白2(BRAP2)在睾丸中高度表达,但其作用在很大程度上尚不清楚。在此,我们通过记录来自人类睾丸的BRAP2相互作用组来解决这个问题,利用酵母双杂交系统鉴定与BRAP2相互作用的蛋白质,这些蛋白质在多种细胞过程中发挥作用,包括肌动蛋白细胞骨架的调节、泛素化、细胞周期/凋亡和转录。通过免疫共沉淀实验证实了成年小鼠睾丸中BRAP2与其中三种蛋白,即PH结构域和富含亮氨酸重复蛋白磷酸酶1(PHLPP1)、A激酶锚定蛋白(AKAP3)和DNA甲基转移酶1(DNMT1)的相互作用。通过定量共聚焦显微镜也证实了BRAP2抑制PHLPP1和DNMT1核定位的能力。重要的是,PHLPP1、AKAP3和DNMT1在粗线期精母细胞/圆形精子细胞中的细胞质定位暗示了其生理相关性,此时BRAP2高水平存在,而PHLPP1和DNMT1在精原细胞中的核定位伴随着较低水平的BRAP2。有趣的是,BRAP2也存在于小鼠精子中,部分与AKAP3共定位。这些结果共同首次表明,BRAP2可能在睾丸生殖细胞中发挥重要的NRNI作用,在成熟精子中还具有额外的支架/结构作用。

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