A nervous system-specific subnuclear organelle in Caenorhabditis elegans
Abstract We describe here phase-separated subnuclear organelles in the nematode Caenorhabditis elegans, which we term NUN (NUclear Nervous system-specific) bodies. Unlike other previously described subnuclear organelles, NUN bodies are highly cell type specific. In fully mature animals, 4–10 NUN bod...
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creator | Pham, Kenneth Masoudi, Neda Leyva-Díaz, Eduardo Hobert, Oliver |
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We describe here phase-separated subnuclear organelles in the nematode Caenorhabditis elegans, which we term NUN (NUclear Nervous system-specific) bodies. Unlike other previously described subnuclear organelles, NUN bodies are highly cell type specific. In fully mature animals, 4–10 NUN bodies are observed exclusively in the nucleus of neuronal, glial and neuron-like cells, but not in other somatic cell types. Based on co-localization and genetic loss of function studies, NUN bodies are not related to other previously described subnuclear organelles, such as nucleoli, splicing speckles, paraspeckles, Polycomb bodies, promyelocytic leukemia bodies, gems, stress-induced nuclear bodies, or clastosomes. NUN bodies form immediately after cell cycle exit, before other signs of overt neuronal differentiation and are unaffected by the genetic elimination of transcription factors that control many other aspects of neuronal identity. In one unusual neuron class, the canal-associated neurons, NUN bodies remodel during larval development, and this remodeling depends on the Prd-type homeobox gene ceh-10. In conclusion, we have characterized here a novel subnuclear organelle whose cell type specificity poses the intriguing question of what biochemical process in the nucleus makes all nervous system-associated cells different from cells outside the nervous system. |
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We describe here phase-separated subnuclear organelles in the nematode Caenorhabditis elegans, which we term NUN (NUclear Nervous system-specific) bodies. Unlike other previously described subnuclear organelles, NUN bodies are highly cell type specific. In fully mature animals, 4–10 NUN bodies are observed exclusively in the nucleus of neuronal, glial and neuron-like cells, but not in other somatic cell types. Based on co-localization and genetic loss of function studies, NUN bodies are not related to other previously described subnuclear organelles, such as nucleoli, splicing speckles, paraspeckles, Polycomb bodies, promyelocytic leukemia bodies, gems, stress-induced nuclear bodies, or clastosomes. NUN bodies form immediately after cell cycle exit, before other signs of overt neuronal differentiation and are unaffected by the genetic elimination of transcription factors that control many other aspects of neuronal identity. In one unusual neuron class, the canal-associated neurons, NUN bodies remodel during larval development, and this remodeling depends on the Prd-type homeobox gene ceh-10. In conclusion, we have characterized here a novel subnuclear organelle whose cell type specificity poses the intriguing question of what biochemical process in the nucleus makes all nervous system-associated cells different from cells outside the nervous system.</description><identifier>ISSN: 1943-2631</identifier><identifier>ISSN: 0016-6731</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/iyaa016</identifier><identifier>PMID: 33683371</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; Caenorhabditis elegans ; Caenorhabditis elegans Proteins - genetics ; Caenorhabditis elegans Proteins - metabolism ; Cell Cycle ; Developmental stages ; Gems ; Genetics ; Homeobox ; Homeodomain Proteins - genetics ; Homeodomain Proteins - metabolism ; Intranuclear Space - metabolism ; Intranuclear Space - ultrastructure ; Investigation ; Larval development ; Leukemia ; Localization ; Nematodes ; Nervous system ; Neuroglia - ultrastructure ; Neuronal-glial interactions ; Neurons - ultrastructure ; Nuclei (cytology) ; Nucleoli ; Organelles ; Polycomb group proteins ; Promyeloid leukemia ; Splicing ; Transcription factors ; Worms</subject><ispartof>Genetics (Austin), 2021-03, Vol.217 (1), p.1-17</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. All rights reserved. For permissions, please email: journals.permissions@oup.com 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. All rights reserved. For permissions, please email: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-4b0ed6b80958451b8b95cbbe48593e8c5efe468e9e28719f17c3191bcd592e893</citedby><cites>FETCH-LOGICAL-c460t-4b0ed6b80958451b8b95cbbe48593e8c5efe468e9e28719f17c3191bcd592e893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33683371$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pham, Kenneth</creatorcontrib><creatorcontrib>Masoudi, Neda</creatorcontrib><creatorcontrib>Leyva-Díaz, Eduardo</creatorcontrib><creatorcontrib>Hobert, Oliver</creatorcontrib><title>A nervous system-specific subnuclear organelle in Caenorhabditis elegans</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>Abstract
We describe here phase-separated subnuclear organelles in the nematode Caenorhabditis elegans, which we term NUN (NUclear Nervous system-specific) bodies. Unlike other previously described subnuclear organelles, NUN bodies are highly cell type specific. In fully mature animals, 4–10 NUN bodies are observed exclusively in the nucleus of neuronal, glial and neuron-like cells, but not in other somatic cell types. Based on co-localization and genetic loss of function studies, NUN bodies are not related to other previously described subnuclear organelles, such as nucleoli, splicing speckles, paraspeckles, Polycomb bodies, promyelocytic leukemia bodies, gems, stress-induced nuclear bodies, or clastosomes. NUN bodies form immediately after cell cycle exit, before other signs of overt neuronal differentiation and are unaffected by the genetic elimination of transcription factors that control many other aspects of neuronal identity. In one unusual neuron class, the canal-associated neurons, NUN bodies remodel during larval development, and this remodeling depends on the Prd-type homeobox gene ceh-10. In conclusion, we have characterized here a novel subnuclear organelle whose cell type specificity poses the intriguing question of what biochemical process in the nucleus makes all nervous system-associated cells different from cells outside the nervous system.</description><subject>Animals</subject><subject>Caenorhabditis elegans</subject><subject>Caenorhabditis elegans Proteins - genetics</subject><subject>Caenorhabditis elegans Proteins - metabolism</subject><subject>Cell Cycle</subject><subject>Developmental stages</subject><subject>Gems</subject><subject>Genetics</subject><subject>Homeobox</subject><subject>Homeodomain Proteins - genetics</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Intranuclear Space - metabolism</subject><subject>Intranuclear Space - ultrastructure</subject><subject>Investigation</subject><subject>Larval development</subject><subject>Leukemia</subject><subject>Localization</subject><subject>Nematodes</subject><subject>Nervous system</subject><subject>Neuroglia - ultrastructure</subject><subject>Neuronal-glial interactions</subject><subject>Neurons - ultrastructure</subject><subject>Nuclei (cytology)</subject><subject>Nucleoli</subject><subject>Organelles</subject><subject>Polycomb group proteins</subject><subject>Promyeloid leukemia</subject><subject>Splicing</subject><subject>Transcription factors</subject><subject>Worms</subject><issn>1943-2631</issn><issn>0016-6731</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1LAzEQxYMoft89yYIXQdYmm2w2uQhS_ALBi55Dks7WyDapyW6h_70prUW9eJqB-c1j3jyEzgi-JljS0RQ89M6mkVtqjQnfQYdEMlpWnJLdH_0BOkrpA2PMZS320QGlXFDakEP0eFt4iIswpCItUw-zMs3ButbZIg3GD7YDHYsQp9pD10HhfDHW4EN812biepcK6CAP0wnaa3WX4HRTj9Hb_d3r-LF8fnl4Gt8-l5Zx3JfMYJhwI3A-hNXECCNrawwwUUsKwtbQAuMCJFSiIbIljaVEEmMntaxASHqMbta688HMYGLB91F3ah7dTMelCtqp3xPv3tU0LJTArG4wyQKXG4EYPgdIvZq5ZLO57DC_QVVMyvwozquMXvxBP8IQfba3ohjFDSUrQbymbAwpRWi3xxCsVjGp75jUJqa8cv7TxHbhO5cMXK2BMMz_l_sCycahkQ</recordid><startdate>20210303</startdate><enddate>20210303</enddate><creator>Pham, Kenneth</creator><creator>Masoudi, Neda</creator><creator>Leyva-Díaz, Eduardo</creator><creator>Hobert, Oliver</creator><general>Oxford University Press</general><general>Genetics Society of America</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>4U-</scope><scope>7QP</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210303</creationdate><title>A nervous system-specific subnuclear organelle in Caenorhabditis elegans</title><author>Pham, Kenneth ; Masoudi, Neda ; Leyva-Díaz, Eduardo ; Hobert, Oliver</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-4b0ed6b80958451b8b95cbbe48593e8c5efe468e9e28719f17c3191bcd592e893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Caenorhabditis elegans</topic><topic>Caenorhabditis elegans Proteins - genetics</topic><topic>Caenorhabditis elegans Proteins - metabolism</topic><topic>Cell Cycle</topic><topic>Developmental stages</topic><topic>Gems</topic><topic>Genetics</topic><topic>Homeobox</topic><topic>Homeodomain Proteins - genetics</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Intranuclear Space - metabolism</topic><topic>Intranuclear Space - ultrastructure</topic><topic>Investigation</topic><topic>Larval development</topic><topic>Leukemia</topic><topic>Localization</topic><topic>Nematodes</topic><topic>Nervous system</topic><topic>Neuroglia - ultrastructure</topic><topic>Neuronal-glial interactions</topic><topic>Neurons - ultrastructure</topic><topic>Nuclei (cytology)</topic><topic>Nucleoli</topic><topic>Organelles</topic><topic>Polycomb group proteins</topic><topic>Promyeloid leukemia</topic><topic>Splicing</topic><topic>Transcription factors</topic><topic>Worms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pham, Kenneth</creatorcontrib><creatorcontrib>Masoudi, Neda</creatorcontrib><creatorcontrib>Leyva-Díaz, Eduardo</creatorcontrib><creatorcontrib>Hobert, Oliver</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetics (Austin)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pham, Kenneth</au><au>Masoudi, Neda</au><au>Leyva-Díaz, Eduardo</au><au>Hobert, Oliver</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A nervous system-specific subnuclear organelle in Caenorhabditis elegans</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>2021-03-03</date><risdate>2021</risdate><volume>217</volume><issue>1</issue><spage>1</spage><epage>17</epage><pages>1-17</pages><issn>1943-2631</issn><issn>0016-6731</issn><eissn>1943-2631</eissn><abstract>Abstract
We describe here phase-separated subnuclear organelles in the nematode Caenorhabditis elegans, which we term NUN (NUclear Nervous system-specific) bodies. Unlike other previously described subnuclear organelles, NUN bodies are highly cell type specific. In fully mature animals, 4–10 NUN bodies are observed exclusively in the nucleus of neuronal, glial and neuron-like cells, but not in other somatic cell types. Based on co-localization and genetic loss of function studies, NUN bodies are not related to other previously described subnuclear organelles, such as nucleoli, splicing speckles, paraspeckles, Polycomb bodies, promyelocytic leukemia bodies, gems, stress-induced nuclear bodies, or clastosomes. NUN bodies form immediately after cell cycle exit, before other signs of overt neuronal differentiation and are unaffected by the genetic elimination of transcription factors that control many other aspects of neuronal identity. In one unusual neuron class, the canal-associated neurons, NUN bodies remodel during larval development, and this remodeling depends on the Prd-type homeobox gene ceh-10. In conclusion, we have characterized here a novel subnuclear organelle whose cell type specificity poses the intriguing question of what biochemical process in the nucleus makes all nervous system-associated cells different from cells outside the nervous system.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>33683371</pmid><doi>10.1093/genetics/iyaa016</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Caenorhabditis elegans Caenorhabditis elegans Proteins - genetics Caenorhabditis elegans Proteins - metabolism Cell Cycle Developmental stages Gems Genetics Homeobox Homeodomain Proteins - genetics Homeodomain Proteins - metabolism Intranuclear Space - metabolism Intranuclear Space - ultrastructure Investigation Larval development Leukemia Localization Nematodes Nervous system Neuroglia - ultrastructure Neuronal-glial interactions Neurons - ultrastructure Nuclei (cytology) Nucleoli Organelles Polycomb group proteins Promyeloid leukemia Splicing Transcription factors Worms |
title | A nervous system-specific subnuclear organelle in Caenorhabditis elegans |
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