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非洲爪蟾前肾中arid5b亚型的差异表达。

Differential expression of arid5b isoforms in Xenopus laevis pronephros.

作者信息

Le Bouffant Ronan, Cunin Anne-Claire, Buisson Isabelle, Cartry Jérôme, Riou Jean-François, Umbhauer Muriel

机构信息

Sorbonne Universités, UPMC Univ Paris 06 and CNRS, UMR7622 Developmental Biology, Paris, France.

出版信息

Int J Dev Biol. 2014;58(5):363-8. doi: 10.1387/ijdb.140029mu.

Abstract

Arid5b belongs to the ARID family of transcription factors characterised by a helix-turn-helix motif- based DNA-binding domain called ARID (A-T Rich Interaction Domain). In human, alternative splicing leads to long and short isoforms (isoform1 and 2, respectively) which differ in their N-terminal part. In this study, we report the cloning and expression pattern of Xenopus laevis arid5b. We have isolated a full length cDNA that shows homology with the human arid5b isoform1. Furthermore, 5'RACE experiments revealed the presence of a shorter isoform equivalent to the human isoform2. Temporal expression analysis by RT-qPCR indicated that X. laevis arid5b isoform1 and isoform2 are differentially expressed during development. Isoform1 is strongly expressed maternally, while isoform2 expression is essentially restricted to tailbud stages. Spatial expression analysis by whole mount in situ showed that arid5b is predominantly expressed in the developing pronephros. Arid5b mRNAs are detected in the antero-dorsal part of the pronephros anlage at the early tailbud stage and later on, in the proximal part of the pronephric tubule. RT-qPCR analyses with primers that allow to discriminate isoform1 from isoform2 showed that the latter is enriched in the pronephros anlage. In agreement with a specific pronephric signature of the isoform2, we also observed that isoform2 but not isoform1 is upregulated in animal caps induced to form pronephric tissue in response to activin A and retinoic acid. These results indicate that the two arid5b isoforms are differentially expressed and likely play different roles during early Xenopus development.

摘要

Arid5b属于转录因子的ARID家族,其特征是具有一个基于螺旋-转角-螺旋基序的DNA结合结构域,称为ARID(富含A-T的相互作用结构域)。在人类中,可变剪接产生了长和短两种异构体(分别为异构体1和2),它们的N端部分有所不同。在本研究中,我们报道了非洲爪蟾arid5b的克隆及表达模式。我们分离出了一个全长cDNA,它与人类arid5b异构体1具有同源性。此外,5'RACE实验揭示了存在一种与人类异构体2等效的较短异构体。通过RT-qPCR进行的时序表达分析表明,非洲爪蟾arid5b异构体1和异构体2在发育过程中差异表达。异构体1在母体内强烈表达,而异构体2的表达基本上仅限于尾芽期。通过整体原位杂交进行的空间表达分析表明,arid5b主要在发育中的前肾中表达。在尾芽早期,在前肾原基的前背侧部分检测到Arid5b mRNA,随后在近端肾小管中也能检测到。用能够区分异构体1和异构体2的引物进行的RT-qPCR分析表明,后者在前肾原基中富集。与异构体2的特定前肾特征一致,我们还观察到,在响应激活素A和视黄酸诱导形成前肾组织的动物帽中,异构体2而非异构体1被上调。这些结果表明,两种arid5b异构体差异表达,并且在非洲爪蟾早期发育过程中可能发挥不同作用。

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