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睾丸细胞中Nectin-2的表达是通过Sp1、CREB和AP-1家族转录因子之间的功能协作来控制的。

Nectin-2 expression in testicular cells is controlled via the functional cooperation between transcription factors of the Sp1, CREB, and AP-1 families.

作者信息

Lui Wing-Yee, Sze Kit-Ling, Lee Will M

机构信息

Department of Zoology, The University of Hong Kong, Pokfulam, Hong Kong.

出版信息

J Cell Physiol. 2006 Apr;207(1):144-57. doi: 10.1002/jcp.20545.

Abstract

Nectin-2, a major protein component of the adherens junctions (AJs), is found between Sertoli cells and germ cells in the seminiferous epithelium. Recent studies have shown that the expression of nectin-2 gene in testis is crucial to maintain normal spermatogenesis since male knockout mice lacking nectin-2 gene are sterile and possess morphologically abnormal spermatozoa. However, the molecular mechanisms governing its basal transcription remain poorly understood. By the use of Sertoli and germ cell-lines (TM4 and GC-2spd(ts) cells, respectively) in transient transfection studies, we showed that the minimal mouse nectin-2 promoter was located between nucleotides -316 and -211 (relative to the translation start site). Two putative Sp1 motifs and one each of the CRE, AP1, and AP2 motifs were identified within this region. Mutational studies showed that these two Sp1 motifs cooperated synergistically with the CRE motif, but not the AP1 and AP2 motifs, to regulate nectin-2 gene transcription in both TM4 and GC-2spd(ts) cells. By EMSAs, we found that an AP-1 consensus sequence was able to inhibit DNA-protein complex formation with the CRE motif, suggesting an interaction between the AP-1 transcription factor (c-Jun) and CREB within the CRE motif. Overexpressions of CREB and c-Jun, but not c-Fos, also significantly increased the promoter activity, which suggests that CREB and c-Jun are the crucial transcription factors involved in regulating nectin-2 gene transcription. Chromatin immunoprecipitation assay has shown that, in vivo, CREB, c-Jun, and Sp1 family proteins are bound to the mouse nectin-2 promoter. Analysis of the staged tubules has confirmed that the cyclic expressions of CREB and nectin-2 coincide with the event of adherens junction restructuring between Sertoli cells and germ cells. The cross-talk between CREB, c-Jun, and Sp1 family protein is believed to be a major transcription machinery to drive nectin-2 expression in Sertoli cells.

摘要

连接黏附分子2(Nectin-2)是黏着连接(AJs)的一种主要蛋白质成分,存在于生精上皮的支持细胞和生殖细胞之间。最近的研究表明,睾丸中Nectin-2基因的表达对于维持正常精子发生至关重要,因为缺乏Nectin-2基因的雄性基因敲除小鼠不育,且精子形态异常。然而,其基础转录的分子机制仍知之甚少。通过在瞬时转染研究中使用支持细胞系和生殖细胞系(分别为TM4和GC-2spd(ts)细胞),我们发现小鼠Nectin-2最小启动子位于核苷酸-316至-211之间(相对于翻译起始位点)。在该区域内鉴定出两个推定的Sp1基序以及一个CRE、一个AP1和一个AP2基序。突变研究表明,这两个Sp1基序与CRE基序协同作用,而非与AP1和AP2基序协同作用,以调节TM4和GC-2spd(ts)细胞中Nectin-2基因的转录。通过电泳迁移率变动分析(EMSA),我们发现一个AP-1共有序列能够抑制与CRE基序的DNA-蛋白质复合物形成,这表明AP-1转录因子(c-Jun)与CRE基序内的CREB之间存在相互作用。CREB和c-Jun的过表达,而非c-Fos的过表达,也显著增加了启动子活性,这表明CREB和c-Jun是参与调节Nectin-2基因转录的关键转录因子。染色质免疫沉淀分析表明,在体内,CREB、c-Jun和Sp1家族蛋白与小鼠Nectin-2启动子结合。对分期生精小管的分析证实,CREB和Nectin-2的周期性表达与支持细胞和生殖细胞之间黏着连接重组事件一致。CREB、c-Jun和Sp1家族蛋白之间的相互作用被认为是驱动支持细胞中Nectin-2表达的主要转录机制。

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