Ma Liman, Wang Wenji, Yang Xiao, Jiang Jiajun, Song Huayu, Jiang Haibin, Zhang Quanqi, Qi Jie
Key Laboratory of Marine Genetics and Breeding, Ministry of Education, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, People's Republic of China.
Fish Physiol Biochem. 2014 Aug;40(4):1263-74. doi: 10.1007/s10695-014-9921-z. Epub 2014 Feb 25.
The Dmrt genes encode a large family of transcription factors with a conserved zinc finger-like DNA-binding DM domain. The function of Dmrt1, one of the family members, in sexual development has been well studied in invertebrates and vertebrates. In the present study, the full-length cDNA of Dmrt1 was isolated from the testis of Sebastes schlegeli. The full-length cDNA of S. schlegeli Dmrt1 (SsDmrt1) was 1,587 bp and contained a 189-bp 5' UTR, a 489-bp 3' UTR and a 909-bp open reading frame, which encoded 302 amino acids with a conserved DM domain and an male-specific motif domain. Phylogenetic analysis showed the evolutionary relationships of SsDmrt1 with other known Dmrt genes in fish and tetrapods. Several transcriptional factor-binding sites in the 5' promoter were identified that might regulate SsDmrt1 expression. Quantitative real-time PCR analysis indicated that SsDmrt1 was expressed in all of the inspected larval developmental stages from 1 to 35 days after birth and that the level of expression gradually decreased. The expression of SsDmrt1 in adult gonads was sexually dimorphic with extremely high expression in the testis, but very low expression in the ovary. No expression was detected in other tissues. Using in situ hybridization, we demonstrated that SsDmrt1 was specifically expressed in the germ cells of both the testis and the ovary. Thus, our results suggest that SsDmrt1 may have an important role in the differentiation of both the testis and the ovary of S. schlegeli.
Dmrt基因编码了一个转录因子大家族,其具有一个保守的锌指样DNA结合DM结构域。该家族成员之一的Dmrt1在无脊椎动物和脊椎动物的性别发育中的功能已得到充分研究。在本研究中,从许氏平鲉的睾丸中分离出了Dmrt1的全长cDNA。许氏平鲉Dmrt1(SsDmrt1)的全长cDNA为1587bp,包含一个189bp的5'非翻译区、一个489bp的3'非翻译区和一个909bp的开放阅读框,其编码302个氨基酸,具有一个保守的DM结构域和一个雄性特异性基序结构域。系统发育分析显示了SsDmrt1与鱼类和四足动物中其他已知Dmrt基因的进化关系。在5'启动子中鉴定出了几个可能调节SsDmrt1表达的转录因子结合位点。定量实时PCR分析表明,SsDmrt1在出生后1至35天的所有检查幼虫发育阶段均有表达,且表达水平逐渐下降。SsDmrt1在成年性腺中的表达具有性别二态性,在睾丸中表达极高,但在卵巢中表达极低。在其他组织中未检测到表达。通过原位杂交,我们证明了SsDmrt1在睾丸和卵巢的生殖细胞中均特异性表达。因此,我们的结果表明,SsDmrt1可能在许氏平鲉睾丸和卵巢的分化中起重要作用。