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PMID: 9885564 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Levels of polyadenylation factor CstF-64 control IgM heavy chain mRNA accumulation and other events associated with B cell differentiation.

Molecular cell ·Vol. 2 ·No. 6 ·1998-12-00 ·Pages 761-71

Takagaki Y, Manley JL

Abstract

Cleavage stimulation factor (CstF) is one of the multiple factors required for mRNA polyadenylation. The concentration of one CstF subunit (CstF-64) increases during activation of B cells, and this is sufficient to switch IgM heavy chain mRNA expression from membrane-bound form to secreted form. To extend this observation, we disrupted the endogenous CstF-64 gene in the B cell line DT40 and replaced it with a regulatable transgene. Strikingly, a 10-fold decrease in CstF-64 concentration did not markedly affect cell growth but specifically and dramatically reduced accumulation of IgM heavy chain mRNA. Further reduction caused reversible cell cycle arrest in G0/G1 phase, while depletion resulted in apoptotic cell death. Our results indicate that CstF-64 plays unexpected roles in regulating gene expression and cell growth in B cells.

MeSH Terms
Animals Apoptosis/physiology B-Lymphocytes/cytology,immunology,metabolism Cell Cycle/physiology Cell Differentiation/genetics,immunology Cell Line Cell Survival/physiology Chickens G1 Phase Gene Expression Regulation Immunoglobulin Heavy Chains/genetics Immunoglobulin M/chemistry,genetics RNA, Messenger/metabolism RNA-Binding Proteins/metabolism,physiology Resting Phase, Cell Cycle mRNA Cleavage and Polyadenylation Factors
Chemicals
Immunoglobulin Heavy Chains Immunoglobulin M RNA, Messenger RNA-Binding Proteins mRNA Cleavage and Polyadenylation Factors
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Takagaki Y
Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
Manley J L
Article Info
Journal
Molecular cell
Abbr.
Mol Cell
ISSN
1097-2765
Published
1998-12-00
Pages
761-71
Language
English
Region
United States
NLM ID
9802571
Subset
IM
Grants
NIGMS NIH HHS · GM 28983 · United States
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