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在海胆(光棘球海胆)中,Otx结合位点是激活HpOtxL mRNA表达所必需的。

The Otx binding site is required for the activation of HpOtxL mRNA expression in the sea urchin, Hemicentrotus pulcherrimus.

作者信息

Hayashibara Yasunori, Mitsunaga-Nakatsubo Keiko, Sakamoto Naoaki, Shimotori Taishin, Akasaka Koji, Yamamoto Takashi

机构信息

Department of Mathematical and Life Sciences, Graduate School of Science, Hiroshima University, Kagamiyama, Higashi-Hiroshima 739-8526, Japan.

出版信息

Dev Growth Differ. 2004 Feb;46(1):61-7. doi: 10.1111/j.1440-169x.2004.00722.x.

Abstract

Two distinct types of orthodenticle-related (HpOtxE and HpOtxL) mRNA are transcribed from a single HpOtx gene by altering the transcription start site and by alternative splicing, and their expressions are differentially regulated during early development of the sea urchin Hemicentrotus pulcherrimus. To understand the mechanism of this regulation, we screened for the enhancer element involved in the stage-specific expression of HpOtxL mRNA. Different portions of the HpOtx gene, including the 5'-flanking region and the first intron, were ligated to the minimal HpOtxL promoter driving a luciferase gene, and their constructs were introduced into fertilized eggs using a particle gun. The enhancer element responsible for proper expression consistent with that of the endogenous HpOtxL was found in the first intron of the HpOtx gene. External and internal deletion analyses showed that the 334 bp region (from +8838 bp to +9171 bp) was required for enhancer activity. In addition, deletion of an Otx binding site within the 334 bp region markedly reduced reporter expression. These results suggest that the Otx binding site within the HpOtxL enhancer is required for the activation of HpOtxL mRNA expression. The promoter preference of the HpOtxL enhancer is also discussed.

摘要

通过改变转录起始位点和选择性剪接,从单个海胆正齿科相关基因(HpOtx)转录出两种不同类型的与正齿科相关的mRNA(HpOtxE和HpOtxL),并且在海胆光棘球海胆早期发育过程中它们的表达受到差异调节。为了理解这种调节机制,我们筛选了参与HpOtxL mRNA阶段特异性表达的增强子元件。将HpOtx基因的不同部分,包括5'侧翼区域和第一个内含子,连接到驱动荧光素酶基因的最小HpOtxL启动子上,并使用粒子枪将它们的构建体导入受精卵中。在HpOtx基因的第一个内含子中发现了负责与内源性HpOtxL表达一致的正确表达的增强子元件。外部和内部缺失分析表明,334 bp区域(从+8838 bp到+9171 bp)是增强子活性所必需的。此外,334 bp区域内Otx结合位点的缺失显著降低了报告基因的表达。这些结果表明,HpOtxL增强子内的Otx结合位点是激活HpOtxL mRNA表达所必需的。还讨论了HpOtxL增强子的启动子偏好性。

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