小鼠睾丸中一个新的Sox5转录物的鉴定

IF 1 4区 生物学 Q4 DEVELOPMENTAL BIOLOGY Gene Expression Patterns Pub Date : 2021-09-01 DOI:10.1016/j.gep.2021.119197
Bangjin Zheng , Chaoyang Huang , Jian Zhou , Lan Ye
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引用次数: 3

摘要

转录因子SOX5在人和小鼠中存在两种不同的亚型,L-SOX5和S-SOX5 (SOX5的长亚型和短亚型)。在这里,我们在小鼠睾丸中鉴定并表征了一种新的Sox5 (S-Sox5变体)转录本。利用基于eclipse的cDNA末端扩增来鉴定潜在的Sox5 mRNA变异。该新转录物与先前报道的S-Sox5在核苷酸序列上具有高度相似性,但具有独特的5'UTR延伸和额外的外显子9。半定量PCR分析显示S-Sox5变异和S-Sox5在小鼠睾丸中特异性表达。这两种转录本在小鼠出生后第21天出现圆形精子时显著增加。我们进一步制作了一系列截断的Sox5构建体,并在HeLa细胞中用eGFP标记它们。体外转染实验发现,SOX5的核定位需要n端和dna结合HMG结构域。本研究结果为进一步研究SOX5在精子发生中的生物学功能奠定了基础。
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Identification of a novel Sox5 transcript in mouse testis

The transcription factor SOX5 is present in two distinct isoforms in both human and mouse, L-SOX5 and S-SOX5 (long and short isoforms of SOX5). Here, we identified and characterized a novel transcript of Sox5 (S-Sox5 variant) in mouse testis. eCLIP-based amplification of cDNA ends were performed to identify the potential Sox5 mRNA variant. This novel transcript shares a high similarity with the previously reported S-Sox5 in nucleotide sequence, but with a unique stretch of 5′UTR and an additional exon 9. Semi-quantitative PCR analysis revealed both S-Sox5 variant and S-Sox5 express specifically in mouse testis. Both transcripts increase significantly in mouse testis at postnatal day 21, when round spermatids appear. We further made a series of truncated Sox5 constructs and tagged them with eGFP in HeLa cells. In vitro transfection assay identified the N-terminus and the DNA-binding HMG domain are required for the nuclear localization of SOX5. Our results provides a basis for the future study to investigate the biological function of SOX5 in spermatogenesis.

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来源期刊
Gene Expression Patterns
Gene Expression Patterns 生物-发育生物学
CiteScore
2.30
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Gene Expression Patterns is devoted to the rapid publication of high quality studies of gene expression in development. Studies using cell culture are also suitable if clearly relevant to development, e.g., analysis of key regulatory genes or of gene sets in the maintenance or differentiation of stem cells. Key areas of interest include: -In-situ studies such as expression patterns of important or interesting genes at all levels, including transcription and protein expression -Temporal studies of large gene sets during development -Transgenic studies to study cell lineage in tissue formation
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