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Characterisation of Caenorhabditis elegans sperm transcriptome and proteome

BACKGROUND: Although sperm is transcriptionally and translationally quiescent, complex populations of RNAs, including mRNAs and non-coding RNAs, exist in sperm. Previous microarray analysis of germ cell mutants identified hundreds of sperm genes in Caenorhabditis elegans. To take a more comprehensiv...

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Autores principales: Ma, Xuan, Zhu, Yingjie, Li, Chunfang, Xue, Peng, Zhao, Yanmei, Chen, Shilin, Yang, Fuquan, Miao, Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028957/
https://www.ncbi.nlm.nih.gov/pubmed/24581041
http://dx.doi.org/10.1186/1471-2164-15-168
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author Ma, Xuan
Zhu, Yingjie
Li, Chunfang
Xue, Peng
Zhao, Yanmei
Chen, Shilin
Yang, Fuquan
Miao, Long
author_facet Ma, Xuan
Zhu, Yingjie
Li, Chunfang
Xue, Peng
Zhao, Yanmei
Chen, Shilin
Yang, Fuquan
Miao, Long
author_sort Ma, Xuan
collection PubMed
description BACKGROUND: Although sperm is transcriptionally and translationally quiescent, complex populations of RNAs, including mRNAs and non-coding RNAs, exist in sperm. Previous microarray analysis of germ cell mutants identified hundreds of sperm genes in Caenorhabditis elegans. To take a more comprehensive view on C. elegans sperm genes, here, we isolate highly pure sperm cells and employ high-throughput technologies to obtain sperm transcriptome and proteome. RESULTS: First, sperm transcriptome consists of considerable amounts of non-coding RNAs, many of which have not been annotated and may play functional roles during spermatogenesis. Second, apart from kinases/phosphatases as previously reported, ion binding proteins are also enriched in sperm, underlying the crucial roles of intracellular ions in post-translational regulation in sperm. Third, while the majority of sperm genes/proteins have low abundance, a small number of sperm genes/proteins are hugely enriched in sperm, implying that sperm only rely on a small set of proteins for post-translational regulation. Lastly, by extensive RNAi screening of sperm enriched genes, we identified a few genes that control fertility. Our further analysis reveals a tight correlation between sperm transcriptome and sperm small RNAome, suggesting that the endogenous siRNAs strongly repress sperm genes. This leads to an idea that the inefficient RNAi screening of sperm genes, a phenomenon currently with unknown causes, might result from the competition between the endogenous RNAi pathway and the exogenous RNAi pathway. CONCLUSIONS: Together, the obtained sperm transcriptome and proteome serve as valuable resources to systematically study spermatogenesis in C. elegans.
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spelling pubmed-40289572014-05-22 Characterisation of Caenorhabditis elegans sperm transcriptome and proteome Ma, Xuan Zhu, Yingjie Li, Chunfang Xue, Peng Zhao, Yanmei Chen, Shilin Yang, Fuquan Miao, Long BMC Genomics Research Article BACKGROUND: Although sperm is transcriptionally and translationally quiescent, complex populations of RNAs, including mRNAs and non-coding RNAs, exist in sperm. Previous microarray analysis of germ cell mutants identified hundreds of sperm genes in Caenorhabditis elegans. To take a more comprehensive view on C. elegans sperm genes, here, we isolate highly pure sperm cells and employ high-throughput technologies to obtain sperm transcriptome and proteome. RESULTS: First, sperm transcriptome consists of considerable amounts of non-coding RNAs, many of which have not been annotated and may play functional roles during spermatogenesis. Second, apart from kinases/phosphatases as previously reported, ion binding proteins are also enriched in sperm, underlying the crucial roles of intracellular ions in post-translational regulation in sperm. Third, while the majority of sperm genes/proteins have low abundance, a small number of sperm genes/proteins are hugely enriched in sperm, implying that sperm only rely on a small set of proteins for post-translational regulation. Lastly, by extensive RNAi screening of sperm enriched genes, we identified a few genes that control fertility. Our further analysis reveals a tight correlation between sperm transcriptome and sperm small RNAome, suggesting that the endogenous siRNAs strongly repress sperm genes. This leads to an idea that the inefficient RNAi screening of sperm genes, a phenomenon currently with unknown causes, might result from the competition between the endogenous RNAi pathway and the exogenous RNAi pathway. CONCLUSIONS: Together, the obtained sperm transcriptome and proteome serve as valuable resources to systematically study spermatogenesis in C. elegans. BioMed Central 2014-02-28 /pmc/articles/PMC4028957/ /pubmed/24581041 http://dx.doi.org/10.1186/1471-2164-15-168 Text en Copyright © 2014 Ma et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ma, Xuan
Zhu, Yingjie
Li, Chunfang
Xue, Peng
Zhao, Yanmei
Chen, Shilin
Yang, Fuquan
Miao, Long
Characterisation of Caenorhabditis elegans sperm transcriptome and proteome
title Characterisation of Caenorhabditis elegans sperm transcriptome and proteome
title_full Characterisation of Caenorhabditis elegans sperm transcriptome and proteome
title_fullStr Characterisation of Caenorhabditis elegans sperm transcriptome and proteome
title_full_unstemmed Characterisation of Caenorhabditis elegans sperm transcriptome and proteome
title_short Characterisation of Caenorhabditis elegans sperm transcriptome and proteome
title_sort characterisation of caenorhabditis elegans sperm transcriptome and proteome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028957/
https://www.ncbi.nlm.nih.gov/pubmed/24581041
http://dx.doi.org/10.1186/1471-2164-15-168
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