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Tgif2基因在编码序列中含有一个保留内含子。

The Tgif2 gene contains a retained intron within the coding sequence.

作者信息

Melhuish Tiffany A, Wotton David

机构信息

Department of Biochemistry and Molecular Genetics, Center for Cell Signaling, University of Virginia, Hospital West, Box 800577, Charlottesville, VA 22908, USA.

出版信息

BMC Mol Biol. 2006 Jan 25;7:2. doi: 10.1186/1471-2199-7-2.

Abstract

BACKGROUND

TGIF and TGIF2 are homeodomain proteins, which act as TGFbeta specific Smad transcriptional corepressors. TGIF recruits general repressors including mSin3 and CtBP. The related TGIF2 protein functions in a similar manner, but does not bind CtBP. In addition to repressing TGFbeta activated gene expression, TGIF and TGIF2 repress gene expression by binding directly to DNA. TGIF and TGIF2 share two major blocks of similarity, encompassing the homeodomain, and a conserved carboxyl terminal repression domain. Here we characterize two splice variants of the Tgif2 gene from mouse and demonstrate that the Tgif2 gene contains a retained intron.

RESULTS

By PCR from mouse cDNA, we identified two alternate splice forms of the Tgif2 gene. One splice variant encodes the full length 237 amino acid Tgif2, whereas the shorter form results in the removal of 39 codons from the centre of the coding region. The generation of this alternate splice form occurs with the mouse RNA, but not the human, and both splice forms are present in all mouse tissues analyzed. Human and mouse Tgif2 coding sequences contain a retained intron, which in mouse Tgif2 is removed by splicing from around 25-50% of RNAs, as assessed by RT-PCR. This splicing event is dependent on sequences within the mouse Tgif2 coding sequence. Both splice forms of mouse Tgif2 encode proteins which are active transcriptional repressors, and can repress both TGFbeta dependent and independent transcription. In addition, we show that human and mouse Tgif2 interact with the transcriptional corepressor mSin3.

CONCLUSION

These data demonstrate that the Tgif2 gene contains a retained intron, within the second coding exon. This retained intron is not removed from the human mRNA at a detectable level, but is spliced out in a significant proportion of mouse RNAs. This alternate splicing is dependent entirely on sequences within the mouse Tgif2 coding sequence, suggesting the presence of an exonic splicing enhancer. Both splice forms of mouse Tgif2 produce proteins which are functional transcriptional repressors.

摘要

背景

TGIF和TGIF2是同源结构域蛋白,作为转化生长因子β(TGFβ)特异性Smad转录共抑制因子发挥作用。TGIF招募包括mSin3和CtBP在内的一般抑制因子。相关的TGIF2蛋白以类似方式发挥功能,但不结合CtBP。除了抑制TGFβ激活的基因表达外,TGIF和TGIF2还通过直接结合DNA来抑制基因表达。TGIF和TGIF2共享两个主要的相似区域,包括同源结构域和一个保守的羧基末端抑制结构域。在此,我们对来自小鼠的Tgif2基因的两种剪接变体进行了表征,并证明Tgif2基因含有一个保留的内含子。

结果

通过从小鼠cDNA进行PCR,我们鉴定出Tgif2基因的两种可变剪接形式。一种剪接变体编码全长237个氨基酸的Tgif2,而较短的形式导致从编码区中心去除39个密码子。这种可变剪接形式的产生发生在小鼠RNA中,而不是人类RNA中,并且两种剪接形式都存在于所有分析的小鼠组织中。人类和小鼠Tgif2编码序列包含一个保留的内含子,通过逆转录聚合酶链反应(RT-PCR)评估,在小鼠Tgif2中,约25%-50%的RNA通过剪接去除了该内含子。这种剪接事件依赖于小鼠Tgif2编码序列内的序列。小鼠Tgif2的两种剪接形式都编码具有活性的转录抑制因子,并且可以抑制TGFβ依赖性和非依赖性转录。此外,我们表明人类和小鼠Tgif2与转录共抑制因子mSin3相互作用。

结论

这些数据表明,Tgif2基因在第二个编码外显子内含有一个保留的内含子。这个保留的内含子在人类mRNA中未以可检测的水平被去除,但在相当比例的小鼠RNA中被剪接掉。这种可变剪接完全依赖于小鼠Tgif2编码序列内的序列,表明存在一个外显子剪接增强子。小鼠Tgif2的两种剪接形式都产生具有功能的转录抑制因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7492/1402312/800edcbfb6af/1471-2199-7-2-1.jpg

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