TAFS AND GENERAL TRANSCRIPTION FACTORS IN YEAST
TAFS AND GENERAL TRANSCRIPTION FACTORS IN YEAST
批准号:
2187476
负责人:
RICHARD YOUNG
金额:
$22.66万
依托单位国家:
美国
项目类别:
财政年份:
1993
资助国家:
美国
项目状态:
已结题
起止时间:
1993-08-01 至 1997-07-31
关键词:
DNA binding protein DNA directed RNA polymerase Saccharomyces cerevisiae fungal genetics gene complementation gene expression genetic promoter element immunoprecipitation laboratory rabbit molecular cloning mutant nucleic acid probes nucleic acid sequence protein sequence recombinant DNA suppressor mutations transcription factor
中文摘要
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英文摘要
The transcription initiation apparatus includes a set of general factors
that associate with promoter DNA and with RNA polymerase II during
initiation. The general transcription factor TFIID is the first to
associate with promoter DNA during assembly of the initiation complex. The
native form of the general transcription factor TFIID consists of the TATA
binding protein (TBP) and multiple TBP-associated factors (TAFs) in higher
eukaryotes, and we have recently found that this is also the case for
yeast. This proposal is designed to identify and clone the genes for the
complete set of Saccharomyces cerevisiae TBP-associated factors, and to
use these genes to pursue molecular genetic and biochemical experiments
designed to elucidate the structure of yeast TFIID and the roles of TAFs
in transcription initiation.
To accomplish these goals, the three specific aims of this proposal are:
i) to isolate genes encoding TBP-associated factors in S. cerevisiae using
genetic and biochemical approaches; 2) to investigate the effects of
mutations on individual TAF functions in vivo; and 3) to study the
function of TAFs and the TBP/TAF complex in vitro. To isolate genes
encoding TAFs, we will continue to exploit a genetic selection that has
already led to the isolation of four TAF genes; the four extragenic
suppressors of RNA polymerase II CTD truncation mutants studied to date
encode TAFs. As a biochemical approach to isolating TAF genes, we will
identify the protein components of a high molecular weight complex
containing TBP, subject these proteins to microsequence analysis, and use
this information to design oligonucleotides for gene isolation. To
investigate the effects of mutations on individual TAF functions in vivo,
we will construct null and conditional mutations in the TAF genes and
analyze their effects on transcription in vivo. To investigate the
functions of the TAFs in the TFIID complex, wild-type and mutant TFIID
preparations will be examined in a variety of transcription assays
designed to assess the role of TAFs in template assembly and commitment
and in basal and activated transcription.
The health relatedness of this research derives from its contribution to
the understanding of the basic molecular mechanisms that control gene
expression.
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海外基金