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雌性先熟的细棘海猪鱼中DMRT1及其假定调控区域的分离与鉴定

Isolation and characterization of DMRT1 and its putative regulatory region in the protogynous wrasse, Halichoeres tenuispinis.

作者信息

Jeong Hyung-Bok, Park Ji-Gweon, Park Young-Ju, Takemura Akihiro, Hur Sung-Pyo, Lee Young-Don, Kim Se-Jae

机构信息

Department of Biology, Jeju National University, 66 Jejudaehakno, Jeju-si, Jeju Special Self-Governing Province, Republic of Korea.

出版信息

Gene. 2009 Jun 1;438(1-2):8-16. doi: 10.1016/j.gene.2009.03.006. Epub 2009 Mar 20.

Abstract

A full-length cDNA of doublesex and mab-3-related transcription factor 1 gene (DMRT1) from wrasse testis was isolated by cDNA library screening. Wrasse DMRT1 was 3116 bp in size and contained the DM domain, with a zinc finger DNA-binding motif, and the male-specific motif. Northern blot analysis identified a 3.2-kb transcript approximately equal in size to the DMRT1 nucleotide sequence detected in the testis, but not in the ovary, confirming that this sequence is male-specific in protogynous wrasse. Southern blot analysis suggested that the wrasse genome contains two copies of the DMRT1 gene. The ORF consisted of five exons and four introns with conserved donor-acceptor splice sites at all exon-intron junctions. The 5'-flanking region of the wrasse DMRT1 gene was isolated by DNA walking, and putative regulatory sites were identified by searching data bases. The 5'-flanking region was divided into 9 elements, then 17 DMRT-luciferase chimeric plasmids were constructed. By transient transfection into Cos-1 and TM4 cells, distal element I which contains GATA-binding sites and proximal element B containing the sex-determining region on Y chromosome gene (SRY) binding site were revealed to have an important role in transcriptional regulation of the wrasse DMRT1 when an enhancer sequence was provided.

摘要

通过cDNA文库筛选,从隆头鱼睾丸中分离出双性与mab - 3相关转录因子1基因(DMRT1)的全长cDNA。隆头鱼DMRT1大小为3116 bp,包含DM结构域,带有锌指DNA结合基序以及雄性特异性基序。Northern印迹分析鉴定出一个3.2 kb的转录本,其大小与在睾丸中检测到的DMRT1核苷酸序列大致相同,但在卵巢中未检测到,这证实了该序列在雌性先熟的隆头鱼中是雄性特异性的。Southern印迹分析表明,隆头鱼基因组包含两个DMRT1基因拷贝。开放阅读框由五个外显子和四个内含子组成,在所有外显子 - 内含子连接处具有保守的供体 - 受体剪接位点。通过DNA步移法分离出隆头鱼DMRT1基因的5'侧翼区域,并通过数据库搜索鉴定出推定的调控位点。5'侧翼区域被分为9个元件,然后构建了17个DMRT - 荧光素酶嵌合质粒。通过瞬时转染到Cos - 1和TM4细胞中,当提供增强子序列时,发现含有GATA结合位点的远端元件I和含有Y染色体性别决定区域基因(SRY)结合位点的近端元件B在隆头鱼DMRT1的转录调控中起重要作用。

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