核糖体分析测序揭示牦牛睾丸发育过程中的翻译动力学

IF 8.5 1区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shaoke Guo , Mengli Cao , Xingdong Wang , Ziqiang Ding , Yandong Kang , Liyan Hu , Ben Zhang , Jie Pei , Xian Guo
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引用次数: 0

摘要

翻译调控在睾丸发育和精子发生中起着至关重要的作用,但其动力学机制尚未阐明。本研究通过核糖体测序(Ribo-seq)整合转录组数据,分析了牦牛(Bos grunniens) 6个月(Y6M)、18个月(Y18M)和4岁(Y4Y)睾丸的翻译情况。结果表明,牦牛的核糖体足迹特征与其他哺乳动物的核糖体足迹特征一致。性成熟期间的差异翻译基因在减数分裂细胞周期、PI3K、Akt和Notch信号通路中显著富集。从Y6M到Y18M,大部分TE改变基因表现出逆转录-翻译效率的趋势,可能与蛋白质泛素化修饰有关。从18m到4Y,翻译改变的基因没有转录变化,但与乙酰转移酶和磷酸转移酶活性相关。PPI分析鉴定出阶段特异性调控基因:COL1A2/MEIOB/SYCP3 (6 M- 18 M)和STAT1/ITGB5/ERBB2 (18 M-4 y)。此外,我们确定了106个预测可翻译的小开放阅读框(sorf),其中包括58个已知编码蛋白和1个长链非编码RNA的注释。序列特征分析表明,较高的翻译效率与较长的uORF长度、较低的GC含量、较短的CDS长度和较高的NMEF有关。本研究结果为研究睾丸发育和精子发生过程中基因翻译的动态调控提供了新的思路,对提高牦牛生殖性能具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ribosome profiling sequencing reveals translational dynamics during yak testicular development
Translation regulation plays a crucial role in testicular development and spermatogenesis, but its dynamic mechanism has not yet been elucidated. This study integrated transcriptome data through ribosomal sequencing (Ribo-seq) to analyze the translation landscape of yak (Bos grunniens) testes at 6 months (Y6M), 18 months (Y18M), and 4 years (Y4Y) of age. The results revealed that the ribosome footprint characteristics of yaks were consistent with those of other mammals. The differentially translated genes during sexual maturity are significantly enriched in the meiotic cell cycle, PI3K Akt, and Notch signaling pathways. From Y6M to Y18M, most of the TE altered genes showed inverse transcription-translation efficiency trends, potentially involved in protein ubiquitination modification. From 18 M to 4Y, translationally altered genes lacked transcriptional changes but associated with acetyltransferase and phosphotransferase activity. PPI analysis identified stage-specific regulatory genes: COL1A2/MEIOB/SYCP3 (6 M–18 M) and STAT1/ITGB5/ERBB2 (18 M-4Y). Additionally, we identified 106 predicted translatable small open reading frames (sORFs), which included annotations for 58 known coding proteins and 1 long non-coding RNA. Sequence feature analysis revealed that higher translation efficiency correlates with longer uORF length, lower GC content, shorter CDS length, and higher NMEF. In conclusion, the results provide new insights into the dynamic regulation of gene translation during testicular development and spermatogenesis, which is highly significant for enhancing yak reproductive performance.
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来源期刊
International Journal of Biological Macromolecules
International Journal of Biological Macromolecules 生物-生化与分子生物学
CiteScore
13.70
自引率
9.80%
发文量
2728
审稿时长
64 days
期刊介绍: The International Journal of Biological Macromolecules is a well-established international journal dedicated to research on the chemical and biological aspects of natural macromolecules. Focusing on proteins, macromolecular carbohydrates, glycoproteins, proteoglycans, lignins, biological poly-acids, and nucleic acids, the journal presents the latest findings in molecular structure, properties, biological activities, interactions, modifications, and functional properties. Papers must offer new and novel insights, encompassing related model systems, structural conformational studies, theoretical developments, and analytical techniques. Each paper is required to primarily focus on at least one named biological macromolecule, reflected in the title, abstract, and text.
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