Molecular mechanisms of extinction: old findings and new ideas

被引:11
作者
Massa, S
Junker, S
Matthias, P
机构
[1] Friedrich Miescher Inst, CH-4058 Basel, Switzerland
[2] Univ Aarhus, Dept Human Genet, DK-8000 Aarhus C, Denmark
关键词
D O I
10.1016/S1357-2725(99)00102-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fusion experiments between somatic cells have been used for a long time as a means to understand the regulation of gene expression. In hybrids between differentiated cells such as hepatocytes or lymphocytes and undifferentiated cells such as fibroblasts a phenomenon called extinction has been: described. In such hybrids expression of cell-specific genes derived from the more differentiated parental cell is selectively turned off (extinguished), whereas genes expressed from both cells like housekeeping genes remain active-after fusion. Study of the molecular basis of extinction:of the liver-specifically expressed tyrosine aminotransferase gene and of the B-cell-specifically expressed immunoglobulin genes has revealed that in hybrids the transcriptional program of the differentiated cells is reset. This is accompanied by a loss of expression or activity of many of the regulatory molecules that were operating in the differentiated cells. In the light of new insights in eukaryotic gene regulation we speculate that molecular mechanisms such as chromatin remodelling, recruitment to heterochromatin or subnuclear localization could underly the extinction process. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:23 / 40
页数:18
相关论文
共 107 条
[31]   Yeast heterochromatin: Regulation of its assembly and inheritance by histones [J].
Grunstein, M .
CELL, 1998, 93 (03) :325-328
[32]   A B-CELL COACTIVATOR OF OCTAMER-BINDING TRANSCRIPTION FACTORS [J].
GSTAIGER, M ;
KNOEPFEL, L ;
GEORGIEV, O ;
SCHAFFNER, W ;
HOVENS, CM .
NATURE, 1995, 373 (6512) :360-362
[33]  
GURDON JB, 1962, J EMBRYOL EXP MORPH, V10, P622
[34]  
GURDON JB, 1986, J CELL SCI, P287
[35]   Helios, a T cell-restricted Ikaros family member that quantitatively associates with Ikaros at centromeric heterochromatin [J].
Hahm, K ;
Cobb, BS ;
McCarty, AS ;
Brown, KE ;
Klug, CA ;
Lee, R ;
Akashi, K ;
Weissman, IL ;
Fisher, AG ;
Smale, ST .
GENES & DEVELOPMENT, 1998, 12 (06) :782-796
[36]   THE POU DOMAIN - A LARGE CONSERVED REGION IN THE MAMMALIAN PIT-1, OCT-1, OCT-2, AND CAENORHABDITIS-ELEGANS UNC-86 GENE-PRODUCTS [J].
HERR, W ;
STURM, RA ;
CLERC, RG ;
CORCORAN, LM ;
BALTIMORE, D ;
SHARP, PA ;
INGRAHAM, HA ;
ROSENFELD, MG ;
FINNEY, M ;
RUVKUN, G ;
HORVITZ, HR .
GENES & DEVELOPMENT, 1988, 2 (12A) :1513-1516
[37]   ACF, an ISWI-containing and ATP-utilizing chromatin assembly and remodeling factor [J].
Ito, T ;
Bulger, M ;
Pazin, MJ ;
Kobayashi, R ;
Kadonaga, JT .
CELL, 1997, 90 (01) :145-155
[38]   POLY(DA-DT), A UBIQUITOUS PROMOTER ELEMENT THAT STIMULATES TRANSCRIPTION VIA ITS INTRINSIC DNA-STRUCTURE [J].
IYER, V ;
STRUHL, K .
EMBO JOURNAL, 1995, 14 (11) :2570-2579
[39]   COOPERATIVITY OF GLUCOCORTICOID RESPONSE ELEMENTS LOCATED FAR UPSTREAM OF THE TYROSINE AMINOTRANSFERASE GENE [J].
JANTZEN, HM ;
STRAHLE, U ;
GLOSS, B ;
STEWART, F ;
SCHMID, W ;
BOSHART, M ;
MIKSICEK, R ;
SCHUTZ, G .
CELL, 1987, 49 (01) :29-38
[40]   COMPLEX PATTERN OF IMMUNOGLOBULIN-MU GENE-EXPRESSION IN NORMAL AND TRANSGENIC MICE - NONOVERLAPPING REGULATORY SEQUENCES GOVERN DISTINCT TISSUE SPECIFICITIES [J].
JENUWEIN, T ;
GROSSCHEDL, R .
GENES & DEVELOPMENT, 1991, 5 (06) :932-943