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通过微阵列分析对鸡精子转录组进行剖析

Chicken sperm transcriptome profiling by microarray analysis.

作者信息

Singh R P, Shafeeque C M, Sharma S K, Singh R, Mohan J, Sastry K V H, Saxena V K, Azeez P A

机构信息

a Avian Physiology and Genetics Division, Sálim Ali Centre for Ornithology and Natural History, Anaikatty-641108, Coimbatore, India.

b Central Avian Research Institute, Izatnagar, 243122, India.

出版信息

Genome. 2016 Mar;59(3):185-96. doi: 10.1139/gen-2015-0106. Epub 2015 Dec 23.

Abstract

It has been confirmed that mammalian sperm contain thousands of functional RNAs, and some of them have vital roles in fertilization and early embryonic development. Therefore, we attempted to characterize transcriptome of the sperm of fertile chickens using microarray analysis. Spermatozoal RNA was pooled from 10 fertile males and used for RNA preparation. Prior to performing the microarray, RNA quality was assessed using a bioanalyzer, and gDNA and somatic cell RNA contamination was assessed by CD4 and PTPRC gene amplification. The chicken sperm transcriptome was cross-examined by analysing sperm and testes RNA on a 4 × 44K chicken array, and results were verified by RT-PCR. Microarray analysis identified 21,639 predominantly nuclear-encoded transcripts in chicken sperm. The majority (66.55%) of the sperm transcripts were shared with the testes, while surprisingly, 33.45% transcripts were detected (raw signal intensity greater than 50) only in the sperm and not in the testes. The greatest proportion of up-regulated transcripts were responsible for signal transduction (63.20%) followed by embryonic development (56.76%) and cell structure (56.25%). Of the 20 most abundant transcripts, 18 remain uncharacterized, whereas the least abundant genes were mostly associated with the ribosome. These findings lay a foundation for more detailed investigations on sperm RNAs in chickens to identify sperm-based biomarkers for fertility.

摘要

已经证实,哺乳动物精子含有数千种功能性RNA,其中一些在受精和早期胚胎发育中起着至关重要的作用。因此,我们试图通过微阵列分析来表征可育鸡精子的转录组。从10只可育雄性鸡中收集精子RNA,并用于RNA制备。在进行微阵列分析之前,使用生物分析仪评估RNA质量,并通过CD4和PTPRC基因扩增评估基因组DNA(gDNA)和体细胞RNA污染。通过在4×44K鸡芯片上分析精子和睾丸RNA来交叉检查鸡精子转录组,并通过逆转录聚合酶链反应(RT-PCR)验证结果。微阵列分析在鸡精子中鉴定出21,639种主要由核编码的转录本。大多数(66.55%)精子转录本与睾丸共有,而令人惊讶的是,33.45%的转录本(原始信号强度大于50)仅在精子中检测到,而在睾丸中未检测到。上调转录本中最大比例负责信号转导(63.20%),其次是胚胎发育(56.76%)和细胞结构(56.25%)。在20种最丰富的转录本中,18种仍未鉴定,而最不丰富的基因大多与核糖体相关。这些发现为更详细地研究鸡精子RNA奠定了基础,以识别基于精子的生育生物标志物。

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