A genome-wide assessment of adrenocorticotropin action in the Y1 mouse adrenal tumor cell line

被引:12
|
作者
Schimmer, Bernard P.
Cordova, Martha
Cheng, Henry
Tsao, Andrew
Morris, Quaid
机构
[1] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M5G 1L6, Canada
[2] Univ Toronto, Dept Pharmacol, Toronto, ON M5G 1L6, Canada
[3] Univ Toronto, Dept Comp Sci, Toronto, ON M5G 1L6, Canada
基金
加拿大健康研究院;
关键词
ACTH; alternative splicing; cAMP; cDNA microarray; protein kinase A; protein kinase C; Y1 mouse adrenocortical tumor cells;
D O I
10.1016/j.mce.2006.12.024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This report summarizes the genome-wide effects of ACTH on transcript accumulation in mouse adrenal Y1 cells and the relative contributions of the cAMP, protein kinase C- and Ca2+-dependent signaling pathways to these actions of the hormone. ACTH affected the accumulation of 1386 transcripts, a much larger number than previously appreciated. The cAMP signaling pathway accounted for approximately 56% of the ACTH effects whereas the protein kinase C- and Ca2+-dependent pathways made smaller contributions to ACTH action. Approximately 38% of the ACTH-affected transcripts could not be assigned to these signaling pathways and thus represent candidates for regulation via other mechanisms. The set of ACTH-regulated transcripts included clusters with functions in steroid metabolism, cell proliferation and alternative splicing. Collectively, our results suggest that Y1 adrenal cells undergo extensive remodeling upon prolonged stimulation with ACTH. The functional implications of ACTH on alternative splicing are explored. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:102 / 107
页数:6
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