Neuroendocrine cell type-specific and inducible expression of chromogranin/secretogranin genes

被引:7
作者
Mahata, SK
Mahapatra, NR
Mahata, M
O'Connor, DT
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] San Diego VA Healthcare Syst, La Jolla, CA 92093 USA
来源
CHROMAFFIN CELL: TRNSMITTER BIOSYNTHESIS, STORAGE, RELEASE, ACTIONS, AND INFORMATICS | 2002年 / 971卷
关键词
chromogranin A; chromogranin B; secretogranin II; catecholamines; PC12; cells;
D O I
10.1111/j.1749-6632.2002.tb04429.x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The chromogranin/secretogranins (Cg/Sg) are a family of soluble, acidic proteins representing major constituents in secretory vesicle cores of virtually all neuroendocrine tissues. We and others have identified the cyclic adenosine monophosphate response element (CRE) as the crucial promoter element responsible for neuroendocrine cell type-specific expression of the Cg/Sg genes. In addition to CRE, GC-rich domains in chromogranin B (Cg/Sg) and serum response element (SRE) in secretogranin II (SgII) promoters appear to play important roles in neuroendocrine cell type-specific expression of CgB and SgII genes. Nicotinic-cholinergic and peptidergic chromaffin cell stimuli evoke catecholamine secretion and augment biosynthesis of Cg/Sg genes. These stimuli signal to CgA gene transcription through the CRE in cis and through protein kinase A, protein kinase C, and mitogen-activated protein kinase and CRE-binding protein in trans. In addition to CRE, a GC-rich domain in CgB and SRE in SgII promoters also play important roles in mediating inducible expression of the CgB and SgII genes. We conclude that CRE, GC-rich domains, and SRE are crucial determinants of both cell type-specific and secretagogue-inducible expression of the Cg/Sg genes.
引用
收藏
页码:27 / 38
页数:12
相关论文
共 60 条
[1]   VASOSTATINS, COMPRISING THE N-TERMINAL DOMAIN OF CHROMOGRANIN-A, SUPPRESS TENSION IN ISOLATED HUMAN BLOOD-VESSEL SEGMENTS [J].
AARDAL, S ;
HELLE, KB ;
ELSAYED, S ;
REED, RK ;
SERCKHANSSEN, G .
JOURNAL OF NEUROENDOCRINOLOGY, 1993, 5 (04) :405-412
[2]   Identification of a novel secretogranin II-derived peptide (SgII187-252) in adult and fetal human adrenal glands using antibodies raised against the human recombinant peptide [J].
Anouar, Y ;
Desmoucelles, C ;
Yon, L ;
Leprince, J ;
Breault, L ;
Gallo-Payet, N ;
Vaudry, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (08) :2944-2951
[3]  
BAUER JW, 1993, J BIOL CHEM, V268, P1586
[4]   PHOSPHORYLATED CREB BINDS SPECIFICALLY TO THE NUCLEAR-PROTEIN CBP [J].
CHRIVIA, JC ;
KWOK, RPS ;
LAMB, N ;
HAGIWARA, M ;
MONTMINY, MR ;
GOODMAN, RH .
NATURE, 1993, 365 (6449) :855-859
[5]   ISOLATION AND PRIMARY STRUCTURE OF A NOVEL CHROMOGRANIN-A-DERIVED PEPTIDE, WE-14, FROM A HUMAN MIDGUT CARCINOID-TUMOR [J].
CURRY, WJ ;
SHAW, C ;
JOHNSTON, CF ;
THIM, L ;
BUCHANAN, KD .
FEBS LETTERS, 1992, 301 (03) :319-321
[6]   Synergistic action of upstream elements and a promoter-proximal CRE is required for neuroendocrine cell-specific expression and second-messenger regulation of the gene encoding the human secretory protein secretogranin II [J].
Desmoucelles, C ;
Vaudry, H ;
Eiden, LE ;
Anouar, Y .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 157 (1-2) :55-66
[7]   CHROMOGRANIN-A SYNTHESIS AND SECRETION IN CHROMAFFIN CELLS [J].
EIDEN, LE ;
IACANGELO, A ;
HSU, CM ;
HOTCHKISS, AJ ;
BADER, MF ;
AUNIS, D .
JOURNAL OF NEUROCHEMISTRY, 1987, 49 (01) :65-74
[8]  
FISCHERCOLBRIE R, 1990, J BIOL CHEM, V265, P9208
[9]   SECRETOGRANIN-II - MOLECULAR-PROPERTIES, REGULATION OF BIOSYNTHESIS AND PROCESSING TO THE NEUROPEPTIDE SECRETONEURIN [J].
FISCHERCOLBRIE, R ;
LASLOP, A ;
KIRCHMAIR, R .
PROGRESS IN NEUROBIOLOGY, 1995, 46 (01) :49-70
[10]   THE GRANIN (CHROMOGRANIN SECRETOGRANIN) FAMILY [J].
HUTTNER, WB ;
GERDES, HH ;
ROSA, P .
TRENDS IN BIOCHEMICAL SCIENCES, 1991, 16 (01) :27-30