Spliced oct-1 mRNA isoforms with untranslated exons and a partly deleted region coding for the POU-specific domain

被引:2
|
作者
Deyev, IE [1 ]
Zhenilo, SV [1 ]
Polanovsky, OL [1 ]
机构
[1] Russian Acad Sci, Engelhardt Inst Mol Biol, Moscow 117984, Russia
关键词
oct-1; mRNA isoforms; alternative splicing; POU domain;
D O I
10.1023/A:1022349216836
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription factor Oct-1 is involved in expression regulation of housekeeping genes, in lymphocyte differentiation, and in the immune response. Tissue-specific Oct-1 mRNA isoforms are known to be expressed in lymphoid cells. Four new mouse isoforms were identified. Of these, two were tissue-specific (oct-1Ralpha and oct-1Rbeta) and contained exon I L. The oct-1Ralpha was shown to contain an additional fragment, which corresponds to an exon located in the Y-region of mouse otf-1. No homolog was found in human OTF-1. The oct-1Rbeta isoform proved to lack an exon coding for a fragment of the POU domain. This deletion results in a loss of the first helix of the domain, and the mutant protein is devoid of affinity for octamer ATGCAAAT. Two other mRNA isoforms, oct-1d and oct-1e, were shown to contain untranslated regions between exons 1U and 2. The regions correspond to exons 1i and 2i located between exons 1U and 1L in the Y-region of the mouse oct-1 gene. Human OTF-1 was not found to contain exon 1i. On evidence of these and published data, it was assumed that a set of Oct-1 isoforms is present in the cell, reflecting the complexity of expression regulation of oct-1 and the multiplicity of its functions.
引用
收藏
页码:125 / 131
页数:7
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