The centrosomal protein pericentrin identified at the basal body complex of the connecting cilium in mouse photoreceptors
Pericentrin (Pcnt), a conserved protein of the pericentriolar material, serves as a multifunctional scaffold for numerous proteins and plays an important role in microtubule organization. Recent studies indicate that Pcnt mutations are associated with a range of diseases including primordial dwarfis...
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description | Pericentrin (Pcnt), a conserved protein of the pericentriolar material, serves as a multifunctional scaffold for numerous proteins and plays an important role in microtubule organization. Recent studies indicate that Pcnt mutations are associated with a range of diseases including primordial dwarfism and ciliopathies. To date, three Pcnt splice variants from orthologous genes in mice and humans are known.
We generated a specific Pcnt antiserum detecting all known Pcnt splice variants and examined the cellular and subcellular distribution of Pcnt in ciliated tissues of the mouse, the olfactory epithelium and the retina. For the first time, we identified Pcnt and its centrosomal interaction partners at the basal body complex of mouse retinal photoreceptors. Photoreceptors are morphologically and functionally subdivided into the light sensitive outer segment and the inner segment comprising the metabolic function of the cell. The two compartments are linked via a modified, specialized, non-motile cilium, the connecting cilium. Here, Pcnt colocalized with the whole protein machinery responsible for transport processes between the two compartments. Surprisingly, photoreceptors expressed a small Pcnt splice transcript - most likely a modified variant of Pcnt S - which was not present in receptor neurons of the olfactory epithelium.
Our findings suggest distinct functional roles of several Pcnt variants in different ciliated tissues and sensory neurons, like the olfactory epithelium and the retina of the mouse. The individual patchwork of different Pcnt splice transcripts seems to reflect the complexity of Pcnt function, an assumption corroborated by the heterogeneous clinical manifestations associated with mutations in the Pcnt gene. |
doi_str_mv | 10.1371/journal.pone.0026496 |
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We generated a specific Pcnt antiserum detecting all known Pcnt splice variants and examined the cellular and subcellular distribution of Pcnt in ciliated tissues of the mouse, the olfactory epithelium and the retina. For the first time, we identified Pcnt and its centrosomal interaction partners at the basal body complex of mouse retinal photoreceptors. Photoreceptors are morphologically and functionally subdivided into the light sensitive outer segment and the inner segment comprising the metabolic function of the cell. The two compartments are linked via a modified, specialized, non-motile cilium, the connecting cilium. Here, Pcnt colocalized with the whole protein machinery responsible for transport processes between the two compartments. Surprisingly, photoreceptors expressed a small Pcnt splice transcript - most likely a modified variant of Pcnt S - which was not present in receptor neurons of the olfactory epithelium.
Our findings suggest distinct functional roles of several Pcnt variants in different ciliated tissues and sensory neurons, like the olfactory epithelium and the retina of the mouse. The individual patchwork of different Pcnt splice transcripts seems to reflect the complexity of Pcnt function, an assumption corroborated by the heterogeneous clinical manifestations associated with mutations in the Pcnt gene.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0026496</identifier><identifier>PMID: 22031837</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alternative splicing ; Animal tissues ; Animals ; Antigens - metabolism ; Biology ; Blotting, Western ; Cell cycle ; Centrosome - metabolism ; Cilia - metabolism ; Compartments ; Complexity ; Disease ; Drosophila ; Dwarfism ; Epithelium ; Fibroblasts ; Genetic aspects ; Insects ; Kinases ; Laser Capture Microdissection ; Localization ; Machinery and equipment ; Medicine ; Mice ; Mice, Inbred C57BL ; Microscopy, Fluorescence ; Microscopy, Immunoelectron ; Mutation ; Neurons ; NIH 3T3 Cells ; Olfactory epithelium ; Olfactory receptor neurons ; Photoreception ; Photoreceptor Cells, Vertebrate - metabolism ; Photoreceptors ; Physiology ; Protein transport ; Proteins ; Retina ; Retina - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Sensory neurons ; Transcription ; Transport processes</subject><ispartof>PloS one, 2011-10, Vol.6 (10), p.e26496-e26496</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Mühlhans et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Mühlhans et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c757t-b1d6e239f27ae5954d8eb690adf9f092f9a3ca7460c7ff567aa64c1a6aa8ae473</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198765/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198765/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22031837$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mühlhans, Johanna</creatorcontrib><creatorcontrib>Brandstätter, Johann Helmut</creatorcontrib><creatorcontrib>Giessl, Andreas</creatorcontrib><title>The centrosomal protein pericentrin identified at the basal body complex of the connecting cilium in mouse photoreceptors</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Pericentrin (Pcnt), a conserved protein of the pericentriolar material, serves as a multifunctional scaffold for numerous proteins and plays an important role in microtubule organization. Recent studies indicate that Pcnt mutations are associated with a range of diseases including primordial dwarfism and ciliopathies. To date, three Pcnt splice variants from orthologous genes in mice and humans are known.
We generated a specific Pcnt antiserum detecting all known Pcnt splice variants and examined the cellular and subcellular distribution of Pcnt in ciliated tissues of the mouse, the olfactory epithelium and the retina. For the first time, we identified Pcnt and its centrosomal interaction partners at the basal body complex of mouse retinal photoreceptors. Photoreceptors are morphologically and functionally subdivided into the light sensitive outer segment and the inner segment comprising the metabolic function of the cell. The two compartments are linked via a modified, specialized, non-motile cilium, the connecting cilium. Here, Pcnt colocalized with the whole protein machinery responsible for transport processes between the two compartments. Surprisingly, photoreceptors expressed a small Pcnt splice transcript - most likely a modified variant of Pcnt S - which was not present in receptor neurons of the olfactory epithelium.
Our findings suggest distinct functional roles of several Pcnt variants in different ciliated tissues and sensory neurons, like the olfactory epithelium and the retina of the mouse. The individual patchwork of different Pcnt splice transcripts seems to reflect the complexity of Pcnt function, an assumption corroborated by the heterogeneous clinical manifestations associated with mutations in the Pcnt gene.</description><subject>Alternative splicing</subject><subject>Animal tissues</subject><subject>Animals</subject><subject>Antigens - metabolism</subject><subject>Biology</subject><subject>Blotting, Western</subject><subject>Cell cycle</subject><subject>Centrosome - metabolism</subject><subject>Cilia - metabolism</subject><subject>Compartments</subject><subject>Complexity</subject><subject>Disease</subject><subject>Drosophila</subject><subject>Dwarfism</subject><subject>Epithelium</subject><subject>Fibroblasts</subject><subject>Genetic aspects</subject><subject>Insects</subject><subject>Kinases</subject><subject>Laser Capture Microdissection</subject><subject>Localization</subject><subject>Machinery and equipment</subject><subject>Medicine</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Fluorescence</subject><subject>Microscopy, Immunoelectron</subject><subject>Mutation</subject><subject>Neurons</subject><subject>NIH 3T3 Cells</subject><subject>Olfactory epithelium</subject><subject>Olfactory receptor neurons</subject><subject>Photoreception</subject><subject>Photoreceptor Cells, Vertebrate - metabolism</subject><subject>Photoreceptors</subject><subject>Physiology</subject><subject>Protein transport</subject><subject>Proteins</subject><subject>Retina</subject><subject>Retina - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Sensory neurons</subject><subject>Transcription</subject><subject>Transport processes</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12L1DAUhoso7rr6D0QLguLFjPlok-ZGWBY_BhYWdPU2pOnJTJa06Tap7Px7MzPdZSp7Ib3I4eR537RverLsNUZLTDn-dOPHoVNu2fsOlggRVgj2JDvFgpIFI4g-PapPshch3CBU0oqx59kJST1cUX6aba83kGvo4uCDb5XL-8FHsF3ew2D3_VTbJhXWWGhyFfOYFLUKia19s821b3sHd7k3-x3tuw50tN0619bZsc2TQevHAHm_8dEPoKFPS3iZPTPKBXg1rWfZr69fri--Ly6vvq0uzi8Xmpc8LmrcMCBUGMIVlKIsmgpqJpBqjDBIECMU1YoXDGluTMm4UqzQWDGlKgUFp2fZ24Nv73yQU2pBYooR4QSXIhGrA9F4dSP7wbZq2EqvrNw3_LCWaohWO5BMU8oFKSjWujC6qKFBjeBE1BwTxE3y-jydNtYtNPsElZuZznc6u5Fr_0dSLCrOymTwYTIY_O0IIcrWBg3OqQ5SilKgCmFCaJHId_-Qj3_cRK1Ven_bGZ-O1TtPeV5wVjFOEUnU8hEqPQ20Nl0pGJv6M8HHmSAxEe7iWo0hyNXPH__PXv2es--P2A0oFzfBuzFa34U5WBxAnf7cMIB5yBgjuRuQ-zTkbkDkNCBJ9ub4fh5E9xNB_wLB2g2K</recordid><startdate>20111021</startdate><enddate>20111021</enddate><creator>Mühlhans, Johanna</creator><creator>Brandstätter, Johann Helmut</creator><creator>Giessl, Andreas</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20111021</creationdate><title>The centrosomal protein pericentrin identified at the basal body complex of the connecting cilium in mouse photoreceptors</title><author>Mühlhans, Johanna ; Brandstätter, Johann Helmut ; Giessl, Andreas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c757t-b1d6e239f27ae5954d8eb690adf9f092f9a3ca7460c7ff567aa64c1a6aa8ae473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Alternative splicing</topic><topic>Animal tissues</topic><topic>Animals</topic><topic>Antigens - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mühlhans, Johanna</au><au>Brandstätter, Johann Helmut</au><au>Giessl, Andreas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The centrosomal protein pericentrin identified at the basal body complex of the connecting cilium in mouse photoreceptors</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-10-21</date><risdate>2011</risdate><volume>6</volume><issue>10</issue><spage>e26496</spage><epage>e26496</epage><pages>e26496-e26496</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Pericentrin (Pcnt), a conserved protein of the pericentriolar material, serves as a multifunctional scaffold for numerous proteins and plays an important role in microtubule organization. Recent studies indicate that Pcnt mutations are associated with a range of diseases including primordial dwarfism and ciliopathies. To date, three Pcnt splice variants from orthologous genes in mice and humans are known.
We generated a specific Pcnt antiserum detecting all known Pcnt splice variants and examined the cellular and subcellular distribution of Pcnt in ciliated tissues of the mouse, the olfactory epithelium and the retina. For the first time, we identified Pcnt and its centrosomal interaction partners at the basal body complex of mouse retinal photoreceptors. Photoreceptors are morphologically and functionally subdivided into the light sensitive outer segment and the inner segment comprising the metabolic function of the cell. The two compartments are linked via a modified, specialized, non-motile cilium, the connecting cilium. Here, Pcnt colocalized with the whole protein machinery responsible for transport processes between the two compartments. Surprisingly, photoreceptors expressed a small Pcnt splice transcript - most likely a modified variant of Pcnt S - which was not present in receptor neurons of the olfactory epithelium.
Our findings suggest distinct functional roles of several Pcnt variants in different ciliated tissues and sensory neurons, like the olfactory epithelium and the retina of the mouse. The individual patchwork of different Pcnt splice transcripts seems to reflect the complexity of Pcnt function, an assumption corroborated by the heterogeneous clinical manifestations associated with mutations in the Pcnt gene.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22031837</pmid><doi>10.1371/journal.pone.0026496</doi><tpages>e26496</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alternative splicing Animal tissues Animals Antigens - metabolism Biology Blotting, Western Cell cycle Centrosome - metabolism Cilia - metabolism Compartments Complexity Disease Drosophila Dwarfism Epithelium Fibroblasts Genetic aspects Insects Kinases Laser Capture Microdissection Localization Machinery and equipment Medicine Mice Mice, Inbred C57BL Microscopy, Fluorescence Microscopy, Immunoelectron Mutation Neurons NIH 3T3 Cells Olfactory epithelium Olfactory receptor neurons Photoreception Photoreceptor Cells, Vertebrate - metabolism Photoreceptors Physiology Protein transport Proteins Retina Retina - metabolism Reverse Transcriptase Polymerase Chain Reaction Sensory neurons Transcription Transport processes |
title | The centrosomal protein pericentrin identified at the basal body complex of the connecting cilium in mouse photoreceptors |
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