Elimination of paternal mitochondria through the lysosomal degradation pathway in C. elegans
In mammals, the inheritance of mitochondrion and its DNA (mtDNA) is strictly maternal, despite the fact that a sperm can inject up to 100 functional mitochondria into the oocyte during fertilization. The mechanisms respon- sible for the elimination of the paternal mitochondria remain largely unknown...
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description | In mammals, the inheritance of mitochondrion and its DNA (mtDNA) is strictly maternal, despite the fact that a sperm can inject up to 100 functional mitochondria into the oocyte during fertilization. The mechanisms respon- sible for the elimination of the paternal mitochondria remain largely unknown. We report here that this paternal mitochondrial elimination process is conserved in Caenorhabditis elegans, and that the lysosomal pathway actively participates in this process. Molecular and cell biological analyses indicate that in wild-type animals paternal mito- chondria and mtDNA are destroyed within two hours after fertilization. In animals with compromised lysosomes, pa- ternal mitochondria persist until late embryonic stages. Therefore, the lysosomal pathway plays an important role in degrading paternal mitochondria introduced into the oocyte during fertilization. Our study indicates that C. elegans is an excellent animal model for understanding and dissecting this conserved biological process critical for animal de- velopment and reproduction. |
doi_str_mv | 10.1038/cr.2011.182 |
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The mechanisms respon- sible for the elimination of the paternal mitochondria remain largely unknown. We report here that this paternal mitochondrial elimination process is conserved in Caenorhabditis elegans, and that the lysosomal pathway actively participates in this process. Molecular and cell biological analyses indicate that in wild-type animals paternal mito- chondria and mtDNA are destroyed within two hours after fertilization. In animals with compromised lysosomes, pa- ternal mitochondria persist until late embryonic stages. Therefore, the lysosomal pathway plays an important role in degrading paternal mitochondria introduced into the oocyte during fertilization. Our study indicates that C. elegans is an excellent animal model for understanding and dissecting this conserved biological process critical for animal de- velopment and reproduction.</description><identifier>ISSN: 1001-0602</identifier><identifier>EISSN: 1748-7838</identifier><identifier>DOI: 10.1038/cr.2011.182</identifier><identifier>PMID: 22105480</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/443/494 ; 631/80/474/1624 ; 631/80/642/333 ; Animal models ; Animals ; Autophagy ; Biological analysis ; Biomedical and Life Sciences ; Caenorhabditis elegans - embryology ; Caenorhabditis elegans Proteins - antagonists & inhibitors ; Caenorhabditis elegans Proteins - genetics ; Caenorhabditis elegans Proteins - metabolism ; Cell Biology ; Deoxyribonucleic acid ; DNA ; DNA, Mitochondrial - metabolism ; Embryo, Nonmammalian - metabolism ; Life Sciences ; Lysosomes - metabolism ; Male ; Mammals ; Mitochondria - metabolism ; mtDNA ; Original ; original-article ; Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors ; Receptors, Cytoplasmic and Nuclear - genetics ; Receptors, Cytoplasmic and Nuclear - metabolism ; RNA Interference ; Time Factors ; Ubiquitin - metabolism ; 受精过程 ; 哺乳动物 ; 溶酶体 ; 父亲 ; 线粒体 ; 线虫 ; 降解途径</subject><ispartof>Cell research, 2011-12, Vol.21 (12), p.1662-1669</ispartof><rights>Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences 2011</rights><rights>Copyright Nature Publishing Group Dec 2011</rights><rights>Copyright © 2011 Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences 2011 Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-ff75bfd0db86203022ff842e981ffb4fbe630ec0c1248fd4b2ea81388a47ec6d3</citedby><cites>FETCH-LOGICAL-c536t-ff75bfd0db86203022ff842e981ffb4fbe630ec0c1248fd4b2ea81388a47ec6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85240X/85240X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234996/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234996/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,41467,42536,51297,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22105480$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Qinghua</creatorcontrib><creatorcontrib>Li, Haimin</creatorcontrib><creatorcontrib>Xue, Ding</creatorcontrib><title>Elimination of paternal mitochondria through the lysosomal degradation pathway in C. elegans</title><title>Cell research</title><addtitle>Cell Res</addtitle><addtitle>Cell Research</addtitle><description>In mammals, the inheritance of mitochondrion and its DNA (mtDNA) is strictly maternal, despite the fact that a sperm can inject up to 100 functional mitochondria into the oocyte during fertilization. The mechanisms respon- sible for the elimination of the paternal mitochondria remain largely unknown. We report here that this paternal mitochondrial elimination process is conserved in Caenorhabditis elegans, and that the lysosomal pathway actively participates in this process. Molecular and cell biological analyses indicate that in wild-type animals paternal mito- chondria and mtDNA are destroyed within two hours after fertilization. In animals with compromised lysosomes, pa- ternal mitochondria persist until late embryonic stages. Therefore, the lysosomal pathway plays an important role in degrading paternal mitochondria introduced into the oocyte during fertilization. Our study indicates that C. elegans is an excellent animal model for understanding and dissecting this conserved biological process critical for animal de- velopment and reproduction.</description><subject>631/443/494</subject><subject>631/80/474/1624</subject><subject>631/80/642/333</subject><subject>Animal models</subject><subject>Animals</subject><subject>Autophagy</subject><subject>Biological analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Caenorhabditis elegans - embryology</subject><subject>Caenorhabditis elegans Proteins - antagonists & inhibitors</subject><subject>Caenorhabditis elegans Proteins - genetics</subject><subject>Caenorhabditis elegans Proteins - metabolism</subject><subject>Cell Biology</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Mitochondrial - metabolism</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Life Sciences</subject><subject>Lysosomes - metabolism</subject><subject>Male</subject><subject>Mammals</subject><subject>Mitochondria - 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embryology</topic><topic>Caenorhabditis elegans Proteins - antagonists & inhibitors</topic><topic>Caenorhabditis elegans Proteins - genetics</topic><topic>Caenorhabditis elegans Proteins - metabolism</topic><topic>Cell Biology</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA, Mitochondrial - metabolism</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Life Sciences</topic><topic>Lysosomes - metabolism</topic><topic>Male</topic><topic>Mammals</topic><topic>Mitochondria - metabolism</topic><topic>mtDNA</topic><topic>Original</topic><topic>original-article</topic><topic>Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors</topic><topic>Receptors, Cytoplasmic and Nuclear - genetics</topic><topic>Receptors, Cytoplasmic and Nuclear - metabolism</topic><topic>RNA Interference</topic><topic>Time Factors</topic><topic>Ubiquitin - metabolism</topic><topic>受精过程</topic><topic>哺乳动物</topic><topic>溶酶体</topic><topic>父亲</topic><topic>线粒体</topic><topic>线虫</topic><topic>降解途径</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Qinghua</creatorcontrib><creatorcontrib>Li, Haimin</creatorcontrib><creatorcontrib>Xue, Ding</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-自然科学</collection><collection>中文科技期刊数据库-自然科学-生物科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Qinghua</au><au>Li, Haimin</au><au>Xue, Ding</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elimination of paternal mitochondria through the lysosomal degradation pathway in C. elegans</atitle><jtitle>Cell research</jtitle><stitle>Cell Res</stitle><addtitle>Cell Research</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>21</volume><issue>12</issue><spage>1662</spage><epage>1669</epage><pages>1662-1669</pages><issn>1001-0602</issn><eissn>1748-7838</eissn><abstract>In mammals, the inheritance of mitochondrion and its DNA (mtDNA) is strictly maternal, despite the fact that a sperm can inject up to 100 functional mitochondria into the oocyte during fertilization. The mechanisms respon- sible for the elimination of the paternal mitochondria remain largely unknown. We report here that this paternal mitochondrial elimination process is conserved in Caenorhabditis elegans, and that the lysosomal pathway actively participates in this process. Molecular and cell biological analyses indicate that in wild-type animals paternal mito- chondria and mtDNA are destroyed within two hours after fertilization. In animals with compromised lysosomes, pa- ternal mitochondria persist until late embryonic stages. Therefore, the lysosomal pathway plays an important role in degrading paternal mitochondria introduced into the oocyte during fertilization. Our study indicates that C. elegans is an excellent animal model for understanding and dissecting this conserved biological process critical for animal de- velopment and reproduction.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>22105480</pmid><doi>10.1038/cr.2011.182</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/443/494 631/80/474/1624 631/80/642/333 Animal models Animals Autophagy Biological analysis Biomedical and Life Sciences Caenorhabditis elegans - embryology Caenorhabditis elegans Proteins - antagonists & inhibitors Caenorhabditis elegans Proteins - genetics Caenorhabditis elegans Proteins - metabolism Cell Biology Deoxyribonucleic acid DNA DNA, Mitochondrial - metabolism Embryo, Nonmammalian - metabolism Life Sciences Lysosomes - metabolism Male Mammals Mitochondria - metabolism mtDNA Original original-article Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors Receptors, Cytoplasmic and Nuclear - genetics Receptors, Cytoplasmic and Nuclear - metabolism RNA Interference Time Factors Ubiquitin - metabolism 受精过程 哺乳动物 溶酶体 父亲 线粒体 线虫 降解途径 |
title | Elimination of paternal mitochondria through the lysosomal degradation pathway in C. elegans |
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