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PMID: 9616132 Published · epublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

New perspectives on retinoblastoma family functions in differentiation.

Frontiers in bioscience : a journal and virtual library ·Vol. 3 ·1998-06-08 ·Pages D532-47

Yee AS, Shih HH, Tevosian SG

Abstract

Cell differentiation is a coordinated process that includes cell cycle exit and the expression of unique genes to specify tissue identity. The focus of this review is the recent progress in understanding the functions of the RB family (RB, p130,p107) in cell differentiation. Much work has focused on the functions of RB in G1 regulation. However, much evidence now suggests a diverse function in differentiation. For discussion, differentiation will be divided into three general steps: cell cycle exit, apoptosis protection, and tissue-specific gene expression. These processes are coordinated to provide the final and unique tissue characteristics. The RB family and targets such as E2F and HBP1 have functions in each step. While there is much knowledge on each separate step of differentiation, the mechanisms that coordinate cell cycle and tissue-specific events are still not known. New evidence suggests that this coordination contains both positive and negative regulation of tissue-specific gene expression. RB. p130, HBP1, and other proteins appear to have unexpected functions in regulating tissue-specific gene expression. The ubiquitous expressions of these proteins suggest membership in a new and general pathway to coordinate cell cycle events with tissue-specific gene expression during differentiation. The collective observations hypothesize the existence of a differentiation checkpoint to insure fidelity.

MeSH Terms
Adipocytes/cytology Animals Apoptosis Carrier Proteins Cell Cycle Cell Cycle Proteins Cell Differentiation Cell Line DNA-Binding Proteins E2F Transcription Factors Gene Expression Regulation High Mobility Group Proteins/physiology Mice Mice, Knockout Muscles/cytology Nuclear Proteins/genetics,physiology Organ Specificity Phosphoproteins/genetics,physiology Proteins Repressor Proteins/physiology Retinoblastoma Protein/genetics,physiology Retinoblastoma-Binding Protein 1 Retinoblastoma-Like Protein p107 Retinoblastoma-Like Protein p130 Transcription Factor DP1 Transcription Factors/physiology
Chemicals
Arid4a protein, mouse Carrier Proteins Cell Cycle Proteins DNA-Binding Proteins E2F Transcription Factors HBP1 protein, human Hbp1 protein, mouse High Mobility Group Proteins Nuclear Proteins Phosphoproteins Proteins Rbl1 protein, mouse Rbl2 protein, mouse Repressor Proteins Retinoblastoma Protein Retinoblastoma-Binding Protein 1 Retinoblastoma-Like Protein p107 Retinoblastoma-Like Protein p130 Transcription Factor DP1 Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yee A S
The Department of Biochemistry, Tufts University School of Medicine, 136 Harrison Ave., Boston, MA 02111, USA. [email protected]
Shih H H
Tevosian S G
Article Info
Journal
Frontiers in bioscience : a journal and virtual library
Abbr.
Front Biosci
ISSN
1093-9946
Published
1998-06-08
Epub
1998-00-08
Pages
D532-47
Language
English
Region
United States
NLM ID
9709506
Subset
IM
Grants
NIGMS NIH HHS · GM44634 · United States
NIDDK NIH HHS · P30 DK-34928 · United States
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