Shim Sangwoo, Bae Narina, Han Jin-Kwan
Laboratory of Developmental Biology, Department of Life Science and Division of Molecular and Life Sciences, Pohang University of Science and Technology, San 31 Hyoja-Dong, Pohang, Kyungbuk, 790-784, South Korea.
Nucleic Acids Res. 2002 Jul 15;30(14):3107-17. doi: 10.1093/nar/gkf437.
We have previously isolated Xretpos, a novel family of long terminal repeat (LTR)-retrotransposons in Xenopus laevis, whose transcript is restricted to ventro-posterior-specific regions and induced by bone morphogenetic protein-4 (BMP-4) signaling. To explore the molecular mechanism of the transcriptional regulation, we identified and characterized Xretpos promoter regions consisting of LTRs and a 5'-untranslated region. We demonstrated that this promoter region contains all the necessary regulatory elements for the spatial and temporal expression of XRETPOS: Sequence analysis of the Xretpos promoter revealed multiple Smad-binding elements and Olf-1/EBF-associated zinc finger (OAZ) binding sites similar to BMP-4 response element, which were identified and proved to be required for BMP-4 induction in the Xvent2 promoter. We further demonstrated that Smads and OAZ proteins bind to their response elements in the promoter and these bindings are essential for the BMP-4-induced activation of the Xretpos promoter. Furthermore, we showed that the endogenous expression of Xretpos protein indeed occurred and was temporally regulated and BMP-4-inducible during the early Xenopus development. Finally, overexpression and partial loss-of-function study revealed that Xretpos has a posterio-ventralizing activity. Together, our results place Xretpos downstream of BMP-4 and provide evidence for the conserved mechanism of transcriptional regulation of the BMP-4 target genes.
我们之前在非洲爪蟾中分离出了Xretpos,它是长末端重复序列(LTR)逆转座子的一个新家族,其转录本局限于腹侧后部特定区域,并由骨形态发生蛋白4(BMP-4)信号诱导。为了探究转录调控的分子机制,我们鉴定并表征了由LTR和5'非翻译区组成的Xretpos启动子区域。我们证明该启动子区域包含XRETPOS空间和时间表达所需的所有调控元件:Xretpos启动子的序列分析揭示了多个Smad结合元件和类似于BMP-4反应元件的Olf-1/EBF相关锌指(OAZ)结合位点,这些位点在Xvent2启动子中被鉴定并证明是BMP-4诱导所必需的。我们进一步证明Smads和OAZ蛋白与启动子中的反应元件结合,这些结合对于BMP-4诱导的Xretpos启动子激活至关重要。此外,我们表明Xretpos蛋白的内源性表达确实发生,并且在非洲爪蟾早期发育过程中受到时间调控且可被BMP-4诱导。最后,过表达和部分功能丧失研究表明Xretpos具有腹侧后部化活性。总之,我们的结果表明Xretpos位于BMP-4下游,并为BMP-4靶基因转录调控的保守机制提供了证据。