Neurosecretion competence. A comprehensive gene expression program identified in PC12 cells

The phenotype of neurosecretory cells is characterized by clear vesicles and dense granules, both discharged by regulated exocytosis. However, these organelles are lacking completely in a few neurosecretion-incompetent clones of the pheochromocytoma PC12 line, in which other specific features are ma...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of biological chemistry 2002-09, Vol.277 (39), p.36715-36724
Hauptverfasser: Grundschober, Christophe, Malosio, Maria Luisa, Astolfi, Laura, Giordano, Tiziana, Nef, Patrick, Meldolesi, Jacopo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 36724
container_issue 39
container_start_page 36715
container_title The Journal of biological chemistry
container_volume 277
creator Grundschober, Christophe
Malosio, Maria Luisa
Astolfi, Laura
Giordano, Tiziana
Nef, Patrick
Meldolesi, Jacopo
description The phenotype of neurosecretory cells is characterized by clear vesicles and dense granules, both discharged by regulated exocytosis. However, these organelles are lacking completely in a few neurosecretion-incompetent clones of the pheochromocytoma PC12 line, in which other specific features are maintained (incompetent clones). In view of the heterogeneity of PC12 cells, a differential characterization of the incompetent phenotype based on the comparison of a single incompetent and a single wild-type clone would have been inconclusive. Therefore, we have compared two pairs of PC12 clones, studying in parallel the transcript levels of 4,200 genes and 19,000 express sequence tags (ESTs) by high density oligonucleotide arrays. After accurate data processing for quality control and filtration, a total of 755 transcripts, corresponding to 448 genes and 307 ESTs, was found consistently changed, with 46% up-regulated and 54% down-regulated in incompetent versus wild-type clones. Many but not all neurosecretion genes were profoundly down-regulated in incompetent cells. Expression of endocytosis genes was normal, whereas that of many nuclear and transcription factors, including some previously shown to play key roles in neurogenesis, was profoundly changed. Additional differences appeared in genes involved in signaling and metabolism. Taken together these results demonstrate for the first time that expression of neurosecretory vesicles and granules is part of a complex gene expression program that includes many other features that so far have not been recognized.
doi_str_mv 10.1074/jbc.M203777200
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_72109608</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18484328</sourcerecordid><originalsourceid>FETCH-LOGICAL-p238t-c27d57cb13dbf5ed634c40efe08c4f41c941b0893a0fec4ed33d0fb284c494a13</originalsourceid><addsrcrecordid>eNqF0DtPwzAQB3APIFoKKyPyxJZyfrR2xqriJZXHABNDlNjn4qpxgp0g-PakUGZuOd3pp9NfR8gZgykDJS83lZnecxBKKQ5wQMYAnGU5n-kROU5pA0PJnB2REeOggM35mLw-YB-bhCZi55tATVO32GEwOKWLnyniG4bkP5CuMSDFz2GT0s62sVnHsqbeYui882ipD_RpyTg1uN2mE3Loym3C032fkJfrq-flbbZ6vLlbLlZZy4XuMsOVnSlTMWErN0M7F9JIQIegjXSSmVyyCnQuSnBoJFohLLiK64HlsmRiQi5-7w6B3ntMXVH7tEtQBmz6VCjOIJ-D_hcyLbUUfAfP97CvarRFG31dxq_i72_iG-T9bog</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18484328</pqid></control><display><type>article</type><title>Neurosecretion competence. A comprehensive gene expression program identified in PC12 cells</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Grundschober, Christophe ; Malosio, Maria Luisa ; Astolfi, Laura ; Giordano, Tiziana ; Nef, Patrick ; Meldolesi, Jacopo</creator><creatorcontrib>Grundschober, Christophe ; Malosio, Maria Luisa ; Astolfi, Laura ; Giordano, Tiziana ; Nef, Patrick ; Meldolesi, Jacopo</creatorcontrib><description>The phenotype of neurosecretory cells is characterized by clear vesicles and dense granules, both discharged by regulated exocytosis. However, these organelles are lacking completely in a few neurosecretion-incompetent clones of the pheochromocytoma PC12 line, in which other specific features are maintained (incompetent clones). In view of the heterogeneity of PC12 cells, a differential characterization of the incompetent phenotype based on the comparison of a single incompetent and a single wild-type clone would have been inconclusive. Therefore, we have compared two pairs of PC12 clones, studying in parallel the transcript levels of 4,200 genes and 19,000 express sequence tags (ESTs) by high density oligonucleotide arrays. After accurate data processing for quality control and filtration, a total of 755 transcripts, corresponding to 448 genes and 307 ESTs, was found consistently changed, with 46% up-regulated and 54% down-regulated in incompetent versus wild-type clones. Many but not all neurosecretion genes were profoundly down-regulated in incompetent cells. Expression of endocytosis genes was normal, whereas that of many nuclear and transcription factors, including some previously shown to play key roles in neurogenesis, was profoundly changed. Additional differences appeared in genes involved in signaling and metabolism. Taken together these results demonstrate for the first time that expression of neurosecretory vesicles and granules is part of a complex gene expression program that includes many other features that so far have not been recognized.</description><identifier>ISSN: 0021-9258</identifier><identifier>DOI: 10.1074/jbc.M203777200</identifier><identifier>PMID: 12070162</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Blotting, Northern ; Cell Line ; Down-Regulation ; Expressed Sequence Tags ; Neurons - metabolism ; Nucleic Acid Hybridization ; Oligonucleotide Array Sequence Analysis ; PC12 Cells ; Rats ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - metabolism ; Statistics as Topic ; Transcription, Genetic ; Up-Regulation</subject><ispartof>The Journal of biological chemistry, 2002-09, Vol.277 (39), p.36715-36724</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12070162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grundschober, Christophe</creatorcontrib><creatorcontrib>Malosio, Maria Luisa</creatorcontrib><creatorcontrib>Astolfi, Laura</creatorcontrib><creatorcontrib>Giordano, Tiziana</creatorcontrib><creatorcontrib>Nef, Patrick</creatorcontrib><creatorcontrib>Meldolesi, Jacopo</creatorcontrib><title>Neurosecretion competence. A comprehensive gene expression program identified in PC12 cells</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The phenotype of neurosecretory cells is characterized by clear vesicles and dense granules, both discharged by regulated exocytosis. However, these organelles are lacking completely in a few neurosecretion-incompetent clones of the pheochromocytoma PC12 line, in which other specific features are maintained (incompetent clones). In view of the heterogeneity of PC12 cells, a differential characterization of the incompetent phenotype based on the comparison of a single incompetent and a single wild-type clone would have been inconclusive. Therefore, we have compared two pairs of PC12 clones, studying in parallel the transcript levels of 4,200 genes and 19,000 express sequence tags (ESTs) by high density oligonucleotide arrays. After accurate data processing for quality control and filtration, a total of 755 transcripts, corresponding to 448 genes and 307 ESTs, was found consistently changed, with 46% up-regulated and 54% down-regulated in incompetent versus wild-type clones. Many but not all neurosecretion genes were profoundly down-regulated in incompetent cells. Expression of endocytosis genes was normal, whereas that of many nuclear and transcription factors, including some previously shown to play key roles in neurogenesis, was profoundly changed. Additional differences appeared in genes involved in signaling and metabolism. Taken together these results demonstrate for the first time that expression of neurosecretory vesicles and granules is part of a complex gene expression program that includes many other features that so far have not been recognized.</description><subject>Animals</subject><subject>Blotting, Northern</subject><subject>Cell Line</subject><subject>Down-Regulation</subject><subject>Expressed Sequence Tags</subject><subject>Neurons - metabolism</subject><subject>Nucleic Acid Hybridization</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>PC12 Cells</subject><subject>Rats</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - metabolism</subject><subject>Statistics as Topic</subject><subject>Transcription, Genetic</subject><subject>Up-Regulation</subject><issn>0021-9258</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0DtPwzAQB3APIFoKKyPyxJZyfrR2xqriJZXHABNDlNjn4qpxgp0g-PakUGZuOd3pp9NfR8gZgykDJS83lZnecxBKKQ5wQMYAnGU5n-kROU5pA0PJnB2REeOggM35mLw-YB-bhCZi55tATVO32GEwOKWLnyniG4bkP5CuMSDFz2GT0s62sVnHsqbeYui882ipD_RpyTg1uN2mE3Loym3C032fkJfrq-flbbZ6vLlbLlZZy4XuMsOVnSlTMWErN0M7F9JIQIegjXSSmVyyCnQuSnBoJFohLLiK64HlsmRiQi5-7w6B3ntMXVH7tEtQBmz6VCjOIJ-D_hcyLbUUfAfP97CvarRFG31dxq_i72_iG-T9bog</recordid><startdate>20020927</startdate><enddate>20020927</enddate><creator>Grundschober, Christophe</creator><creator>Malosio, Maria Luisa</creator><creator>Astolfi, Laura</creator><creator>Giordano, Tiziana</creator><creator>Nef, Patrick</creator><creator>Meldolesi, Jacopo</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20020927</creationdate><title>Neurosecretion competence. A comprehensive gene expression program identified in PC12 cells</title><author>Grundschober, Christophe ; Malosio, Maria Luisa ; Astolfi, Laura ; Giordano, Tiziana ; Nef, Patrick ; Meldolesi, Jacopo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p238t-c27d57cb13dbf5ed634c40efe08c4f41c941b0893a0fec4ed33d0fb284c494a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Blotting, Northern</topic><topic>Cell Line</topic><topic>Down-Regulation</topic><topic>Expressed Sequence Tags</topic><topic>Neurons - metabolism</topic><topic>Nucleic Acid Hybridization</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>PC12 Cells</topic><topic>Rats</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - metabolism</topic><topic>Statistics as Topic</topic><topic>Transcription, Genetic</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grundschober, Christophe</creatorcontrib><creatorcontrib>Malosio, Maria Luisa</creatorcontrib><creatorcontrib>Astolfi, Laura</creatorcontrib><creatorcontrib>Giordano, Tiziana</creatorcontrib><creatorcontrib>Nef, Patrick</creatorcontrib><creatorcontrib>Meldolesi, Jacopo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grundschober, Christophe</au><au>Malosio, Maria Luisa</au><au>Astolfi, Laura</au><au>Giordano, Tiziana</au><au>Nef, Patrick</au><au>Meldolesi, Jacopo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurosecretion competence. A comprehensive gene expression program identified in PC12 cells</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2002-09-27</date><risdate>2002</risdate><volume>277</volume><issue>39</issue><spage>36715</spage><epage>36724</epage><pages>36715-36724</pages><issn>0021-9258</issn><abstract>The phenotype of neurosecretory cells is characterized by clear vesicles and dense granules, both discharged by regulated exocytosis. However, these organelles are lacking completely in a few neurosecretion-incompetent clones of the pheochromocytoma PC12 line, in which other specific features are maintained (incompetent clones). In view of the heterogeneity of PC12 cells, a differential characterization of the incompetent phenotype based on the comparison of a single incompetent and a single wild-type clone would have been inconclusive. Therefore, we have compared two pairs of PC12 clones, studying in parallel the transcript levels of 4,200 genes and 19,000 express sequence tags (ESTs) by high density oligonucleotide arrays. After accurate data processing for quality control and filtration, a total of 755 transcripts, corresponding to 448 genes and 307 ESTs, was found consistently changed, with 46% up-regulated and 54% down-regulated in incompetent versus wild-type clones. Many but not all neurosecretion genes were profoundly down-regulated in incompetent cells. Expression of endocytosis genes was normal, whereas that of many nuclear and transcription factors, including some previously shown to play key roles in neurogenesis, was profoundly changed. Additional differences appeared in genes involved in signaling and metabolism. Taken together these results demonstrate for the first time that expression of neurosecretory vesicles and granules is part of a complex gene expression program that includes many other features that so far have not been recognized.</abstract><cop>United States</cop><pmid>12070162</pmid><doi>10.1074/jbc.M203777200</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 2002-09, Vol.277 (39), p.36715-36724
issn 0021-9258
language eng
recordid cdi_proquest_miscellaneous_72109608
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Animals
Blotting, Northern
Cell Line
Down-Regulation
Expressed Sequence Tags
Neurons - metabolism
Nucleic Acid Hybridization
Oligonucleotide Array Sequence Analysis
PC12 Cells
Rats
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - metabolism
Statistics as Topic
Transcription, Genetic
Up-Regulation
title Neurosecretion competence. A comprehensive gene expression program identified in PC12 cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T14%3A11%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Neurosecretion%20competence.%20A%20comprehensive%20gene%20expression%20program%20identified%20in%20PC12%20cells&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Grundschober,%20Christophe&rft.date=2002-09-27&rft.volume=277&rft.issue=39&rft.spage=36715&rft.epage=36724&rft.pages=36715-36724&rft.issn=0021-9258&rft_id=info:doi/10.1074/jbc.M203777200&rft_dat=%3Cproquest_pubme%3E18484328%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18484328&rft_id=info:pmid/12070162&rfr_iscdi=true