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小鼠ADP核糖基化因子样4基因:两个独立的启动子指导组织和睾丸生殖细胞中的特异性转录。

The mouse ADP-ribosylation factor-like 4 gene: two separate promoters direct specific transcription in tissues and testicular germ cell.

作者信息

Jacobs S, Schürmann A, Becker W, Böckers T M, Copeland N G, Jenkins N A, Joost H G

机构信息

Institut für Pharmakologie und Toxikologie, Medizinische Fakultät der Rheinisch-Westfälischen Technischen Hochschule Aachen, Wendlingweg 2, D-52057 Aachen, Germany.

出版信息

Biochem J. 1998 Oct 15;335 ( Pt 2)(Pt 2):259-65. doi: 10.1042/bj3350259.

Abstract

ADP-ribosylation factor-like protein 4 (ARL4) is a Ras-related GTPase that has been cloned from the 3T3-L1 preadipocyte cell line as an adipocyte-specific cDNA [Schürmann, Breiner, Becker, Huppertz, Kainulainen, Kentrup and Joost (1994) J. Biol. Chem. 269, 15683-15688]. The Arl4 gene maps to the proximal region of mouse chromosome 12 linked to Lamb1-1, Hfhbf1 and Sos2. Compared with all other known genes of Ras-related GTPases, the genomic organization of Arl4 is unusual in that its entire coding region, the 3' untranslated region (UTR) and most of the 5' UTR are located on a single exon. This structure suggests that Arl4 has evolved by retroposition of an Arf (ADP-ribosylation factor) or Arf-like gene. Isolation of the 5' UTR by rapid amplification of cDNA ends (RACE)-PCR revealed heterogeneous transcription initiation sites in alternative exons 1. Both 5'-flanking regions exhibited promoter activity when expressed in COS-7 cells, indicating that the expression of Arl4 is directed by two separate promoters. mRNA transcribed under the control of the downstream promoter was isolated by RACE-PCR from all investigated tissues. In contrast, the upstream promoter seems to drive specifically the expression of Arl4 in adult testis. Hybridization of rat testis in situ indicated that Arl4 is expressed in germ cells of puberal and adult testis, but not in prepuberal testis, suggesting that Arl4 is involved in sperm production.

摘要

ADP-核糖基化因子样蛋白4(ARL4)是一种与Ras相关的GTP酶,已从3T3-L1前脂肪细胞系中作为脂肪细胞特异性cDNA克隆出来[舒尔曼、布雷纳、贝克尔、胡珀茨、凯努莱宁、肯特鲁普和约斯特(1994年)《生物化学杂志》269卷,第15683 - 15688页]。Arl4基因定位于小鼠12号染色体近端区域,与Lamb1-1、Hfhbf1和Sos2连锁。与所有其他已知的Ras相关GTP酶基因相比,Arl4的基因组结构不同寻常,其整个编码区、3'非翻译区(UTR)和大部分5'UTR都位于单个外显子上。这种结构表明Arl4是通过Arf(ADP-核糖基化因子)或Arf样基因的逆转座而进化的。通过cDNA末端快速扩增(RACE)-PCR分离5'UTR,揭示了在替代外显子1中存在异质转录起始位点。当在COS-7细胞中表达时,两个5'侧翼区域均表现出启动子活性,表明Arl4的表达由两个独立的启动子调控。通过RACE-PCR从所有研究组织中分离出在下游启动子控制下转录的mRNA。相比之下,上游启动子似乎特异性地驱动Arl4在成年睾丸中的表达。大鼠睾丸原位杂交表明,Arl4在青春期和成年睾丸的生殖细胞中表达,但在青春期前睾丸中不表达,这表明Arl4参与精子生成。

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