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- Publisher Website: 10.1210/en.2004-1508
- Scopus: eid_2-s2.0-23844438359
- PMID: 15932934
- WOS: WOS:000231243600020
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Article: Modulation of calmodulin gene expression as a novel mechanism for growth hormone feedback control by insulin-like growth factor in grass carp pituitary cells
Title | Modulation of calmodulin gene expression as a novel mechanism for growth hormone feedback control by insulin-like growth factor in grass carp pituitary cells |
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Authors | |
Keywords | Calcineurin Calmidazolium Calmodulin Gene Expression Grass Carp Growth Hormone Insulin-like Growth Factor Pituitary Cells |
Issue Date | 2005 |
Publisher | The Endocrine Society. The Journal's web site is located at http://endo.endojournals.org |
Citation | Endocrinology, 2005, v. 146 n. 9, p. 3821-3835 How to Cite? |
Abstract | Calmodulin (CaM), the Ca2+ sensor in living cells, is essential for biological functions mediated by Ca2+-dependent mechanisms. However, modulation of CaM gene expression at the pituitary level as a means to regulate pituitary hormone synthesis has not been characterized. Here we examined the functional role of CaM in the feedback control of growth hormone (GH) by insulin-like growth factor (IGF) using grass carp pituitary cells as a cell model. To establish the structural identity of CaM expressed in the grass carp, a CaM cDNA, CaM-L, was isolated from the carp pituitary using 3′/5′ RACE. The ORF of this cDNA encodes a 149 a.a. protein sharing the same primary structure with CaMs reported in mammals, birds, and amphibians. This CaM cDNA is phylogenetically related to the CaM I gene family and its transcripts are ubiquitously expressed in the grass carp. In carp pituitary cells, IGF-I and -II induced CaM mRNA expression with a concurrent drop in GH transcript levels. These stimulatory effects on CaM mRNA levels were not mimicked by insulin and appeared to be a direct consequence of IGF activation of CaM gene transcription without altering CaM transcript stability. CaM antagonism and inactivation of calcineurin blocked the inhibitory effects of IGF-I and -II on GH gene expression and CaM over-expression also suppressed the 5′ promoter activity of grass carp GH gene. These results, as a whole, provide evidence for the first time that IGF feedback on GH gene expression is mediated by activation of CaM gene expression at the pituitary level. Copyright © 2005 by The Endocrine Society. |
Persistent Identifier | http://hdl.handle.net/10722/84813 |
ISSN | 2023 Impact Factor: 3.8 2023 SCImago Journal Rankings: 1.285 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Huo, L | en_HK |
dc.contributor.author | Fu, G | en_HK |
dc.contributor.author | Wang, X | en_HK |
dc.contributor.author | Ko, WKW | en_HK |
dc.contributor.author | Wong, AOL | en_HK |
dc.date.accessioned | 2010-09-06T08:57:25Z | - |
dc.date.available | 2010-09-06T08:57:25Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Endocrinology, 2005, v. 146 n. 9, p. 3821-3835 | en_HK |
dc.identifier.issn | 0013-7227 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/84813 | - |
dc.description.abstract | Calmodulin (CaM), the Ca2+ sensor in living cells, is essential for biological functions mediated by Ca2+-dependent mechanisms. However, modulation of CaM gene expression at the pituitary level as a means to regulate pituitary hormone synthesis has not been characterized. Here we examined the functional role of CaM in the feedback control of growth hormone (GH) by insulin-like growth factor (IGF) using grass carp pituitary cells as a cell model. To establish the structural identity of CaM expressed in the grass carp, a CaM cDNA, CaM-L, was isolated from the carp pituitary using 3′/5′ RACE. The ORF of this cDNA encodes a 149 a.a. protein sharing the same primary structure with CaMs reported in mammals, birds, and amphibians. This CaM cDNA is phylogenetically related to the CaM I gene family and its transcripts are ubiquitously expressed in the grass carp. In carp pituitary cells, IGF-I and -II induced CaM mRNA expression with a concurrent drop in GH transcript levels. These stimulatory effects on CaM mRNA levels were not mimicked by insulin and appeared to be a direct consequence of IGF activation of CaM gene transcription without altering CaM transcript stability. CaM antagonism and inactivation of calcineurin blocked the inhibitory effects of IGF-I and -II on GH gene expression and CaM over-expression also suppressed the 5′ promoter activity of grass carp GH gene. These results, as a whole, provide evidence for the first time that IGF feedback on GH gene expression is mediated by activation of CaM gene expression at the pituitary level. Copyright © 2005 by The Endocrine Society. | en_HK |
dc.language | eng | en_HK |
dc.publisher | The Endocrine Society. The Journal's web site is located at http://endo.endojournals.org | en_HK |
dc.relation.ispartof | Endocrinology | en_HK |
dc.rights | Endocrinology. Copyright © The Endocrine Society. | en_HK |
dc.subject | Calcineurin | en_HK |
dc.subject | Calmidazolium | en_HK |
dc.subject | Calmodulin | en_HK |
dc.subject | Gene Expression | en_HK |
dc.subject | Grass Carp | en_HK |
dc.subject | Growth Hormone | en_HK |
dc.subject | Insulin-like Growth Factor | en_HK |
dc.subject | Pituitary Cells | en_HK |
dc.title | Modulation of calmodulin gene expression as a novel mechanism for growth hormone feedback control by insulin-like growth factor in grass carp pituitary cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0013-7227&volume=146&spage=3821&epage=3835&date=2005&atitle=Modulation+of+Calmodulin+Gene+Expression+as+a+Novel+Mechanism+for+Growth+Hormone+Feedback+Control+by+Insulin-like+Growth+Factor+in+Grass+Carp+Pituitary+Cells | en_HK |
dc.identifier.email | Wong, AOL: olwong@hkucc.hku.hk | en_HK |
dc.identifier.authority | Wong, AOL=rp00806 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1210/en.2004-1508 | en_HK |
dc.identifier.pmid | 15932934 | en_HK |
dc.identifier.scopus | eid_2-s2.0-23844438359 | en_HK |
dc.identifier.hkuros | 101435 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-23844438359&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 146 | en_HK |
dc.identifier.issue | 9 | en_HK |
dc.identifier.spage | 3821 | en_HK |
dc.identifier.epage | 3835 | en_HK |
dc.identifier.isi | WOS:000231243600020 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Huo, L=9275343500 | en_HK |
dc.identifier.scopusauthorid | Fu, G=8670614700 | en_HK |
dc.identifier.scopusauthorid | Wang, X=8941883500 | en_HK |
dc.identifier.scopusauthorid | Ko, WKW=7202286890 | en_HK |
dc.identifier.scopusauthorid | Wong, AOL=7403147570 | en_HK |
dc.identifier.issnl | 0013-7227 | - |