Megakaryocyte polyploidization is associated with a functional gene amplification

被引:61
作者
Raslova, H
Roy, L
Vourc'h, C
Le Couedic, JP
Brison, O
Metivier, D
Feunteun, J
Kroemer, G
Debili, N
Vainchenker, W
机构
[1] Inst Gustave Roussy, INSERM, U362, F-94805 Villejuif, France
[2] Inst Gustave Roussy, CNRS, UMR 1599, F-94805 Villejuif, France
[3] INSERM, U309, Inst Albert Bonniot, La Tronche, France
关键词
D O I
10.1182/blood-2002-05-1553
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is believed that polyploidy induces an orchestrated increase in gene expression. To know whether all alleles remain functional during megakaryocyte polyploidization, we used a well-established fluorescence in situ hybridization technique which allows one to simultaneously detect pre-mRNAs and assess ploidy level in a single cell. All alleles of GPIIb, GPIIIa, VWF, beta-actin, hsp70, c-mpl, Fli-1, and FOG-1 genes are transcriptionally active in megakaryocytes from 4N to 32N. All X chromosomes in male cells are transcriptionally active but only half of them are transcriptionally active in female megakaryocytes, as revealed by the transcriptional activity of the GATA-1 gene. Nuclear untranslated XIST RNA accumulates on the inactivated X chromosomes, indicating that they are subjected to a normal inactivation process. Altogether, our results demonstrate that megakaryocyte polyploidization results in a functional gene amplification whose likely function is an increase in protein synthesis parallel with cell enlargement. (C) 2003 by The American Society of Hematology.
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收藏
页码:541 / 544
页数:4
相关论文
共 27 条
[1]   CHARACTERIZATION OF A MURINE GENE EXPRESSED FROM THE INACTIVE X-CHROMOSOME [J].
BORSANI, G ;
TONLORENZI, R ;
SIMMLER, MC ;
DANDOLO, L ;
ARNAUD, D ;
CAPRA, V ;
GROMPE, M ;
PIZZUTI, A ;
MUZNY, D ;
LAWRENCE, C ;
WILLARD, HF ;
AVNER, P ;
BALLABIO, A .
NATURE, 1991, 351 (6324) :325-329
[2]   CONSERVATION OF POSITION AND EXCLUSIVE EXPRESSION OF MOUSE XIST FROM THE INACTIVE X-CHROMOSOME [J].
BROCKDORFF, N ;
ASHWORTH, A ;
KAY, GF ;
COOPER, P ;
SMITH, S ;
MCCABE, VM ;
NORRIS, DP ;
PENNY, GD ;
PATEL, D ;
RASTAN, S .
NATURE, 1991, 351 (6324) :329-331
[3]   THE PRODUCT OF THE MOUSE XIST GENE IS A 15 KB INACTIVE X-SPECIFIC TRANSCRIPT CONTAINING NO CONSERVED ORF AND LOCATED IN THE NUCLEUS [J].
BROCKDORFF, N ;
ASHWORTH, A ;
KAY, GF ;
MCCABE, VM ;
NORRIS, DP ;
COOPER, PJ ;
SWIFT, S ;
RASTAN, S .
CELL, 1992, 71 (03) :515-526
[4]   A GENE FROM THE REGION OF THE HUMAN X-INACTIVATION CENTER IS EXPRESSED EXCLUSIVELY FROM THE INACTIVE X-CHROMOSOME [J].
BROWN, CJ ;
BALLABIO, A ;
RUPERT, JL ;
LAFRENIERE, RG ;
GROMPE, M ;
TONLORENZI, R ;
WILLARD, HF .
NATURE, 1991, 349 (6304) :38-44
[5]   Stabilization and localization of Xist RNA are controlled by separate mechanisms and are not sufficient for X inactivation [J].
Clemson, CM ;
Chow, JC ;
Brown, CJ ;
Lawrence, JB .
JOURNAL OF CELL BIOLOGY, 1998, 142 (01) :13-23
[6]   Phenotypic instability and rapid gene silencing in newly formed arabidopsis allotetraploids [J].
Comai, L ;
Tyagi, AP ;
Winter, K ;
Holmes-Davis, R ;
Reynolds, SH ;
Stevens, Y ;
Byers, B .
PLANT CELL, 2000, 12 (09) :1551-1567
[7]   Inefficient processing impairs release of RNA from the site of transcription [J].
Custódio, N ;
Carmo-Fonseca, M ;
Geraghty, F ;
Pereira, HS ;
Grosveld, F ;
Antoniou, M .
EMBO JOURNAL, 1999, 18 (10) :2855-2866
[8]   EFFECTS OF THE RECOMBINANT HEMATOPOIETIC GROWTH-FACTORS INTERLEUKIN-3, INTERLEUKIN-6, STEM-CELL FACTOR, AND LEUKEMIA INHIBITORY FACTOR ON THE MEGAKARYOCYTIC DIFFERENTIATION OF CD34+ CELLS [J].
DEBILI, N ;
MASSE, JM ;
KATZ, A ;
GUICHARD, J ;
BRETONGORIUS, J ;
VAINCHENKER, W .
BLOOD, 1993, 82 (01) :84-95
[9]   Ploidy regulation of gene expression [J].
Galitski, T ;
Saldanha, AJ ;
Styles, CA ;
Lander, ES ;
Fink, GR .
SCIENCE, 1999, 285 (5425) :251-254
[10]  
GEWIRTZ AM, 1991, HEMATOLOGY BASIC PRI, P1148