Sense and antisense Foxl2 transcripts in mouse

被引:33
作者
Cocquet, J
Pannetier, M
Fellous, M
Veitia, RA
机构
[1] Hop Cochin, INSERM, E0021, F-75014 Paris, France
[2] Hop Cochin, INSERM, U361, F-75014 Paris, France
[3] INRA, Biol Dev & Reprod, Jouy En Josas, France
关键词
FOXL2; antisense RNA; ovarian development; alternative splicing; alternative polyadenylation;
D O I
10.1016/j.ygeno.2005.01.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
FOXL2 is a forkhead transcription factor involved in eyelid development and in the development and adult function of the ovary in mammals. In mouse, we have previously suggested the existence of two mRNA isoforms of Foxl2 that result from an alternative polyadenylation. In this study, we characterize in depth the structure and expression of these two variants. We also describe an antisense transcript that overlaps the whole Foxl2 transcription unit. This antisense transcript, called Foxl2OS (for opposite strand), yields several isoforrns resulting from alternative splicing. No significant coding region was found in the Foxl2OS sequence. Foxl2OS displays a pattern of expression very similar to that of Foxl2 in the gonads during development and at the adult age. RNA FISH experiments show that both transcripts are expressed in the same cells at the same time. We suggest that Foxl2OS is a noncoding antisense RNA that may be involved in the regulation of Foxl2. All in all our results provide new insights about the organization of the marine Foxl2 locus. This might help us understand its regulation and function. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:531 / 541
页数:11
相关论文
共 25 条
[1]   An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation [J].
Baron, D ;
Cocquet, J ;
Xia, XH ;
Fellous, M ;
Guiguen, Y ;
Veitia, RA .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2004, 33 (03) :705-715
[2]   Long-distance chromatin mechanisms controlling tissue-specific gene locus activation [J].
Bonifer, C .
GENE, 1999, 238 (02) :277-289
[3]  
Capaccioli S, 1996, ONCOGENE, V13, P105
[4]   Structure, evolution and expression of the FOXL2 transcription unit [J].
Cocquet, J ;
De Baere, E ;
Gareil, M ;
Pannetier, M ;
Xia, X ;
Fellous, M ;
Veitia, RA .
CYTOGENETIC AND GENOME RESEARCH, 2003, 101 (3-4) :206-211
[5]   Evolution and expression of FOXL2 [J].
Cocquet, J ;
Pailhoux, E ;
Jaubert, F ;
Servel, N ;
Xia, X ;
Pannetier, M ;
De Baere, E ;
Messiaen, L ;
Cotinot, C ;
Fellous, M ;
Veitia, RA .
JOURNAL OF MEDICAL GENETICS, 2002, 39 (12) :916-921
[6]   The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome [J].
Crisponi, L ;
Deiana, M ;
Loi, A ;
Chiappe, F ;
Uda, M ;
Amati, P ;
Bisceglia, L ;
Zelante, L ;
Nagaraja, R ;
Porcu, S ;
Ristaldi, MS ;
Marzella, R ;
Rocchi, M ;
Nicolino, M ;
Lienhardt-Roussie, A ;
Nivelon, A ;
Verloes, A ;
Schlessinger, D ;
Gasparini, P ;
Bonneau, D ;
Cao, A ;
Pilia, G .
NATURE GENETICS, 2001, 27 (02) :159-166
[7]   Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation [J].
De Baere, E ;
Dixon, MJ ;
Small, KW ;
Jabs, EW ;
Leroy, BP ;
Devriendt, K ;
Gillerot, Y ;
Mortier, G ;
Meire, F ;
Van Maldergem, L ;
Courtens, W ;
Hjalgrim, H ;
Huang, S ;
Liebaers, I ;
Van Regemorter, N ;
Touraine, P ;
Praphanphoj, V ;
Verloes, A ;
Udar, N ;
Yellore, V ;
Chalukya, M ;
Yelchits, S ;
De Paepe, A ;
Kuttenn, F ;
Fellous, M ;
Veitia, R ;
Messiaen, L .
HUMAN MOLECULAR GENETICS, 2001, 10 (15) :1591-1600
[8]   Ovarian granulosa cell tumors express a functional membrane receptor for anti-Mullerian hormone in transgenic mice [J].
Dutertre, M ;
Gouédard, L ;
Xavier, F ;
Long, WQ ;
di Clemente, N ;
Picard, JY ;
Rey, R .
ENDOCRINOLOGY, 2001, 142 (09) :4040-4046
[9]   Alternative poly(A) site selection in complex transcription units: Means to an end? [J].
EdwaldsGilbert, G ;
Veraldi, KL ;
Milcarek, C .
NUCLEIC ACIDS RESEARCH, 1997, 25 (13) :2547-2561
[10]   The murine Wilms tumor suppressor gene (wt1) locus [J].
Gong, YL ;
Eggert, H ;
Englert, C .
GENE, 2001, 279 (02) :119-126