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在c-erbAα基因座中鉴定从内部启动子起始的转录本,这些转录本编码视黄酸受体α和三碘甲状腺原氨酸受体活性的抑制剂。

Identification of transcripts initiated from an internal promoter in the c-erbA alpha locus that encode inhibitors of retinoic acid receptor-alpha and triiodothyronine receptor activities.

作者信息

Chassande O, Fraichard A, Gauthier K, Flamant F, Legrand C, Savatier P, Laudet V, Samarut J

机构信息

Laboratoire de Biologie Moléculaire et Cellulaire, Centre Nationale dela Recherche Scientifique UMR 49, Institut Nationale de la Recherche Agronomique LA 913, Ecole Normale Supérieure de Lyon, France.

出版信息

Mol Endocrinol. 1997 Aug;11(9):1278-90. doi: 10.1210/mend.11.9.9972.

Abstract

The thyroid hormone receptor-coding locus, c-erbA alpha, generates several mRNAs originating from a single primary transcript that undergoes alternative splicing. We have identified for the first time two new transcripts, called TRdelta alpha1 and TRdelta alpha2 [mRNA for isoform alpha1 and alpha2 of the T3 receptor (TR), respectively], whose transcription is initiated from an internal promoter located within intron 7 of the c-erbA alpha gene. These two new transcripts exhibit tissue-specific patterns of expression in the mouse. These two patterns are in sharp contrast with the expression patterns of the full-length transcripts generated from the c-erbA alpha locus. TR alpha1 and TRdelta alpha2 mRNAs encode N-terminally truncated isoforms of T3R alpha1 and T3R alpha2, respectively. The protein product of TRdelta alpha1 antagonizes the transcriptional activation elicited by T3 and retinoic acid. This protein inhibits the ligand-induced activating functions of T3R alpha1 and 9-cis-retinoic acid receptor-alpha but does not affect the retinoic acid-dependent activating function of retinoic acid receptor-alpha. We predict that these truncated proteins may work as down-regulators of transcriptional activity of nuclear hormone receptors in vivo.

摘要

甲状腺激素受体编码基因座c-erbAα产生几种源自单个初级转录本的mRNA,该初级转录本会发生可变剪接。我们首次鉴定出两种新的转录本,分别称为TRδα1和TRδα2 [分别为T3受体(TR)的α1和α2亚型的mRNA],它们的转录起始于位于c-erbAα基因第7内含子内的内部启动子。这两种新转录本在小鼠中表现出组织特异性的表达模式。这两种模式与c-erbAα基因座产生的全长转录本的表达模式形成鲜明对比。TRα1和TRδα2 mRNA分别编码T3Rα1和T3Rα2的N端截短亚型。TRδα1的蛋白质产物拮抗T3和视黄酸引发的转录激活。该蛋白抑制配体诱导的T3Rα1和9-顺式视黄酸受体α的激活功能,但不影响视黄酸受体α的视黄酸依赖性激活功能。我们预测这些截短的蛋白可能在体内作为核激素受体转录活性的下调因子发挥作用。

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