Mouillet Jean-François, Yan Xiaomei, Ou Qinglin, Jin Lingling, Muglia Louis J, Crawford Peter A, Sadovsky Yoel
Department of Obstetrics and Gynecology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Endocrinology. 2008 May;149(5):2168-75. doi: 10.1210/en.2007-1237. Epub 2008 Feb 7.
The DEAD-box helicase DP103 (Ddx20, Gemin3) is a multifunctional protein that interacts with Epstein-Barr virus nuclear proteins (EBNA2/EBNA3) and is a part of the spliceosomal small nuclear ribonucleoproteins complex. DP103 also aggregates with the micro-RNA machinery complex. We have previously shown that DP103 interacts with the nuclear receptor steroidogenic factor-1 (SF-1, NR5A1), a key regulator of reproductive development, and represses its transcriptional activity. To further explore the physiological function of DP103, we disrupted the corresponding gene in mice. Homozygous Dp103-null mice die early in embryonic development before a four-cell stage. Although heterozygous mice are healthy and fertile, analysis of steroidogenic tissues revealed minor abnormalities in mutant females, including larger ovaries, altered estrous cycle, and reduced basal secretion of ACTH. Our data point to diverse functions of murine DP103, with an obligatory role during early embryonic development and also in modulation of steroidogenesis.
DEAD盒解旋酶DP103(Ddx20,Gemin3)是一种多功能蛋白,它与爱泼斯坦-巴尔病毒核蛋白(EBNA2/EBNA3)相互作用,并且是剪接体小核核糖核蛋白复合物的一部分。DP103还与微小RNA机制复合物聚集。我们之前已经表明,DP103与核受体类固醇生成因子-1(SF-1,NR5A1)相互作用,SF-1是生殖发育的关键调节因子,DP103会抑制其转录活性。为了进一步探究DP103的生理功能,我们在小鼠中破坏了相应基因。纯合Dp103基因敲除小鼠在胚胎发育早期的四细胞阶段之前就死亡了。虽然杂合小鼠健康且可育,但对类固醇生成组织的分析显示,突变雌性小鼠存在一些轻微异常,包括卵巢更大、发情周期改变以及促肾上腺皮质激素基础分泌减少。我们的数据表明,小鼠DP103具有多种功能,在早期胚胎发育过程中以及类固醇生成调节中都起着必不可少的作用。