4.6 Article

Alternative Splicing Isoforms of Porcine CREB Are Differentially Involved in Transcriptional Transactivation

期刊

GENES
卷 13, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/genes13081304

关键词

pig; CREB; alternative splicing variants; function; RNA-seq

资金

  1. Heilongjiang Science Fund for Distinguished Young Scholars [JQ2020C005]

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The study found that alternative splicing occurs in pig CREB genes, and two isoforms, V1 and V2, have similar roles but exhibit gene-specific effects. Additionally, V3 has no effect on gene expression, while V4 acts as a repressor. The different mechanisms underlying the roles of V1 and V2 were identified through RNA-seq, and specific genes regulated by them were identified.
The cAMP response element-binding protein (CREB), a basic leucine zipper transcription factor, is involved in the activation of numerous genes in a variety of cell types. The CREB gene is rich in alternative splicing (AS) events. However, studies on the AS of CREB genes in pigs are limited, and few reports have compared the roles of isoforms in activating gene expression. Here, five AS transcripts, V1-5, were characterized by RT-PCR and two, V3 and V5, were new identifications. Both V1 and V2 have all the functional domains of the CREB protein, with similar tissue expression profiles and mRNA stability, suggesting that they have similar roles. The transcriptional transactivation activities of four isoforms encoding complete polypeptides were analyzed on the expression of the B-cell CLL/lymphoma 2-like protein 2 and the poly (A)-binding protein, nuclear 1 genes with a dual-luciferase reporter system, and differential activities were observed. Both V1 and V2 have promoting effects, but their roles are gene-specific. V3 has no effect on the promoter of the two genes, while V4 functions as a repressor. The mechanisms underlying the differential roles of V1 and V2 were analyzed with RNA-seq, and the genes specifically regulated by V1 and V2 were identified. These results will contribute to further revealing the role of CREB and to analyzing the significance of AS in genes.

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