Distinct requirements for C-elegans TAFIIs in early embryonic transcription

被引:38
作者
Walker, AK
Rothman, JH
Shi, Y
Blackwell, TK
机构
[1] Harvard Univ, Sch Med, Ctr Blood Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[4] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
关键词
C; elegans; gene regulation; TAF(II)s; TFIID; transcription;
D O I
10.1093/emboj/20.18.5269
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
TAF(II)s are conserved components of the TFIID, TFTC and SAGA-related mRNA transcription complexes. In yeast (y), yTAF(II)17 is required broadly for transcription, but various other TAF(II)s appear to have more specialized functions. It is important to determine how TAF(II)s contribute to transcription in metazoans, which have larger and more diverse genomes. We have examined TAF(II) functions in early Caenorhabditis elegans embryos, which can survive without transcription for several cell generations. We show that taf-10 (yTAF(II)7) and taf-11 (yTAF(II)25) are required for a significant fraction of transcription, but apparently are not needed for expression of multiple developmental and other metazoan-specific genes. In contrast, taf-5 (yTAF(II)48; human TAF(II)130) seems to be required for essentially all early embryonic mRNA transcription. We conclude that TAF-10 and TAF-11 have modular functions in metazoans, and can be bypassed at many metazoan-specific genes. The broad involvement of TAF-5 in mRNA transcription in vivo suggests a requirement for either TFIID or a TFTC-like complex.
引用
收藏
页码:5269 / 5279
页数:11
相关论文
共 72 条
[1]   Ordered recruitment of chromatin modifying and general transcription factors to the IFN-β promoter [J].
Agalioti, T ;
Lomvardas, S ;
Parekh, B ;
Yie, JM ;
Maniatis, T ;
Thanos, D .
CELL, 2000, 103 (04) :667-678
[2]   TAFs revisited: more data reveal new twists and confirm old ideas [J].
Albright, SR ;
Tjian, R .
GENE, 2000, 242 (1-2) :1-13
[3]   Three-dimensional structure of the human TFIID-IIA-IIB complex [J].
Andel, F ;
Ladurner, AG ;
Inouye, C ;
Tjian, R ;
Nogales, E .
SCIENCE, 1999, 286 (5447) :2153-2156
[4]   Genes encoding Drosophila melanogaster RNA polymerase II general transcription factors:: Diversity in TFIIA and TFIID components contributes to gene-specific transcriptional regulation [J].
Aoyagi, N ;
Wassarman, DA .
JOURNAL OF CELL BIOLOGY, 2000, 150 (02) :F45-F49
[5]   Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA [J].
Apone, LM ;
Virbasius, CA ;
Holstege, FCP ;
Wang, J ;
Young, RA ;
Green, MR .
MOLECULAR CELL, 1998, 2 (05) :653-661
[6]   Phosphorylation of the RNA polymerase II largest subunit during Xenopus laevis oocyte maturation [J].
Bellier, S ;
Dubois, MF ;
Nishida, E ;
Almouzni, G ;
Bensaude, O .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1434-1440
[7]   Three-dimensional structures of the TAFII-containing complexes TFIID and TFTC [J].
Brand, M ;
Leurent, C ;
Mallouh, V ;
Tora, L ;
Schultz, P .
SCIENCE, 1999, 286 (5447) :2151-2153
[8]   Identification of TATA-binding protein-free TAFII-containing complex subunits suggests a role in nucleosome acetylation and signal transduction [J].
Brand, M ;
Yamamoto, K ;
Staub, A ;
Tora, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (26) :18285-18289
[9]   TRANSCRIPTION-DEPENDENT REDISTRIBUTION OF THE LARGE SUBUNIT OF RNA-POLYMERASE-II TO DISCRETE NUCLEAR DOMAINS [J].
BREGMAN, DB ;
DU, L ;
VANDERZEE, S ;
WARREN, SL .
JOURNAL OF CELL BIOLOGY, 1995, 129 (02) :287-298
[10]  
BRENNER S, 1974, GENETICS, V77, P71