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关键的垂体 microRNAs 通过调节剪接因子来介导猪 GHRHR 剪接变异体的表达。

Key pituitary miRNAs mediate the expression of pig GHRHR splice variants by regulating splice factors.

机构信息

College of Animal Science, Jilin University, Changchun, Jilin 130062, China.

NHC Key Laboratory of Radiobiology, College of Public Health, Jilin University, Changchun 130021, China.

出版信息

Int J Biol Macromol. 2022 May 31;208:208-218. doi: 10.1016/j.ijbiomac.2022.03.070. Epub 2022 Mar 16.

Abstract

The growth hormone releasing hormone receptor (GHRHR) is well documented in organism growth and its alternative splicing may generate multiple functional GHRHR splice variants (SVs). Our previous study has demonstrated the key pituitary miRNAs (let-7e and miR-328-5p) in pig regulated the expression of GHRHR SVs by directly targeting to them. And according to recent reports, the interplay between miRNA-based silencing of mRNAs and alternative splicing of pre-mRNAs is a crucial post-transcriptional mechanism. In this study, SF3B3 and CPSF4 were firstly excavated as the splice factors that involved in the formation of GHRHR SVs mediated by let-7e and miR-328-5p through the comparation of the expression relations of GHRHR SVs, let-7e/miR-328-5p and SF3B3/CPSF4 in pituitary tissues between Landrace pigs and BaMa pigs, as well as the prediction of the target relations of let-7e/miR-328-5p with SF3B3 and/or CPSF4. SF3B3 and CPSF4 targeted by let-7e and miR-328-5p were further verified by performing dual-luciferase reporter assays and detecting the expression of target transcripts. Then the RT-PCR, RT-qPCR and Western blot assays were used to confirm SF3B3 and CPSF4 were involved in the formation of the GHRHR SVs, and in this process, let-7e and miR-328-5p mediated GHRHR SVs by regulating SF3B3 and CPSF4. Finally, the target site of SF3B3 on pre-GHRHR was on the Exon 12 to Exon14, while CPSF4 acted on the other fragments of the pre-GHRHR, which were explored by dual-luciferase reporter system preliminarily. To the best of our knowledge, this paper is the first to report the miRNAs regulate GHRHR SVs indirectly by splice factors.

摘要

生长激素释放激素受体 (GHRHR) 在生物体生长中得到了充分的证实,其选择性剪接可能产生多种功能性 GHRHR 剪接变异体 (SVs)。我们之前的研究表明,猪的关键垂体 microRNA(let-7e 和 miR-328-5p)通过直接靶向它们来调节 GHRHR SVs 的表达。根据最近的报道,miRNA 介导的 mRNA 沉默和前体 mRNA 选择性剪接之间的相互作用是一种关键的转录后机制。在这项研究中,SF3B3 和 CPSF4 首先被挖掘出来,作为通过 let-7e 和 miR-328-5p 介导的 GHRHR SVs 的剪接因子,这是通过比较长白猪和巴马猪垂体组织中 GHRHR SVs、let-7e/miR-328-5p 和 SF3B3/CPSF4 的表达关系,以及 let-7e/miR-328-5p 与 SF3B3 和/或 CPSF4 的靶关系预测得出的。通过进行双荧光素酶报告基因检测和检测靶转录本的表达,进一步验证了 let-7e 和 miR-328-5p 靶向的 SF3B3 和 CPSF4。然后使用 RT-PCR、RT-qPCR 和 Western blot 检测来确认 SF3B3 和 CPSF4 参与了 GHRHR SVs 的形成,在此过程中,let-7e 和 miR-328-5p 通过调节 SF3B3 和 CPSF4 来介导 GHRHR SVs。最后,通过双荧光素酶报告系统初步探索了 SF3B3 在前 GHRHR 上的靶位点在 Exon 12 到 Exon14,而 CPSF4 作用于前 GHRHR 的其他片段。据我们所知,这是第一篇报道 miRNA 通过剪接因子间接调节 GHRHR SVs 的论文。

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