The bovine calpastatin gene promoter and a novel N-terminal region of the protein are targets forcAMP-dependent protein kinase activity

Persistent Link:
http://hdl.handle.net/10150/288832
Title:
The bovine calpastatin gene promoter and a novel N-terminal region of the protein are targets forcAMP-dependent protein kinase activity
Author:
Cong, Mei, 1966-
Issue Date:
1998
Publisher:
The University of Arizona.
Rights:
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Abstract:
To investigate the regulation of calpastatin gene expression, bovine heart calpastatin cDNAs and 5' regions of the calpastatin gene were isolated. Analysis of 5' cDNA sequence identified a new translation initiation site that is in frame and 204 nucleotides upstream of the previously designated start site. Conceptual translation from this upstream AUG produces a protein containing 68 additional N-terminal amino acids. This "XL" region contains three potential PKA phosphorylation sites but shares no homology with other regions of calpastatin or with any known protein. Immunoblot studies demonstrated that heart and liver contain a calpastatin protein of 145 kDa on SDS PAGE that comigrates with full length bacterially-expressed calpastatin and calpastatin produced by coupled in vitro transcription-translation from the upstream AUG. An antibody raised against the XL region recognized the 145 kDa band, demonstrating that the upstream AUG is utilized and that the 145 kDa band represents full length calpastatin protein in vivo. The organization of the calpastatin 5' genomic region was determined by comparing calpastatin cDNA and genomic sequences. The region encompassing exon 1-4 contains large introns and spans at least 60 kb. Calpastatin promoter sequence analysis revealed that it belong to the family of "house keeping" genes which lack TATA box and are GC rich at the proximal promoter regions. Transient transfection assays demonstrated that sequence within 272 nucleotides upstream of transcription initiation of the calpastatin gene is sufficient to direct moderate level transcription. Promoter sequences further upstream act to inhibit and stimulate transcriptional activity. Exposure of transfected cells to dibutryl cAMP resulted in a seven to twenty fold increase in calpastatin promoter activity for constructs containing at least 272 nucleotides of upstream promoter sequence. Deletion and mutation analyses identified a cAMP responsive element at nt-76. These findings demonstrate that calpastatin gene and protein are both targets for cAMP-dependent kinase activity. beta-Agonist treatment can induce both calpastatin gene transcription and protein phosphorylation.
Type:
text; Dissertation-Reproduction (electronic)
Keywords:
Biology, Molecular.
Degree Name:
Ph.D.
Degree Level:
doctoral
Degree Program:
Graduate College; Biochemistry
Degree Grantor:
University of Arizona
Advisor:
Antin, Parker B.; Goll, Darrel E.

Full metadata record

DC FieldValue Language
dc.language.isoen_USen_US
dc.titleThe bovine calpastatin gene promoter and a novel N-terminal region of the protein are targets forcAMP-dependent protein kinase activityen_US
dc.creatorCong, Mei, 1966-en_US
dc.contributor.authorCong, Mei, 1966-en_US
dc.date.issued1998en_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.description.abstractTo investigate the regulation of calpastatin gene expression, bovine heart calpastatin cDNAs and 5' regions of the calpastatin gene were isolated. Analysis of 5' cDNA sequence identified a new translation initiation site that is in frame and 204 nucleotides upstream of the previously designated start site. Conceptual translation from this upstream AUG produces a protein containing 68 additional N-terminal amino acids. This "XL" region contains three potential PKA phosphorylation sites but shares no homology with other regions of calpastatin or with any known protein. Immunoblot studies demonstrated that heart and liver contain a calpastatin protein of 145 kDa on SDS PAGE that comigrates with full length bacterially-expressed calpastatin and calpastatin produced by coupled in vitro transcription-translation from the upstream AUG. An antibody raised against the XL region recognized the 145 kDa band, demonstrating that the upstream AUG is utilized and that the 145 kDa band represents full length calpastatin protein in vivo. The organization of the calpastatin 5' genomic region was determined by comparing calpastatin cDNA and genomic sequences. The region encompassing exon 1-4 contains large introns and spans at least 60 kb. Calpastatin promoter sequence analysis revealed that it belong to the family of "house keeping" genes which lack TATA box and are GC rich at the proximal promoter regions. Transient transfection assays demonstrated that sequence within 272 nucleotides upstream of transcription initiation of the calpastatin gene is sufficient to direct moderate level transcription. Promoter sequences further upstream act to inhibit and stimulate transcriptional activity. Exposure of transfected cells to dibutryl cAMP resulted in a seven to twenty fold increase in calpastatin promoter activity for constructs containing at least 272 nucleotides of upstream promoter sequence. Deletion and mutation analyses identified a cAMP responsive element at nt-76. These findings demonstrate that calpastatin gene and protein are both targets for cAMP-dependent kinase activity. beta-Agonist treatment can induce both calpastatin gene transcription and protein phosphorylation.en_US
dc.typetexten_US
dc.typeDissertation-Reproduction (electronic)en_US
dc.subjectBiology, Molecular.en_US
thesis.degree.namePh.D.en_US
thesis.degree.leveldoctoralen_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.disciplineBiochemistryen_US
thesis.degree.grantorUniversity of Arizonaen_US
dc.contributor.advisorAntin, Parker B.en_US
dc.contributor.advisorGoll, Darrel E.en_US
dc.identifier.proquest9831833en_US
dc.identifier.bibrecord.b38635896en_US
All Items in UA Campus Repository are protected by copyright, with all rights reserved, unless otherwise indicated.