RNA POL II POLY-A SITE AND 3' TERMINATION
RNA POL II POLY-A SITE AND 3' TERMINATION
批准号:
2634673
负责人:
ERIK S FALCK-PEDERSEN
金额:
$32.44万
依托单位国家:
美国
项目类别:
财政年份:
1990
资助国家:
美国
项目状态:
已结题
起止时间:
1990-01-01 至 1999-12-31
关键词:
DNA directed RNA polymerase RNA splicing electrophoresis genetic regulation genetic terminator element globin molecular cloning nucleic acid metabolism nucleic acid structure oligonucleotides polyadenylate posttranscriptional RNA processing precursor mRNA ribozymes tissue /cell culture transcription termination
中文摘要
这是本建议和我本人的长期总体目标
英文摘要
It is the long term general objective of this proposal and of my
laboratory to understand gene regulation through poly(A) site use in
complex transcription units. For all pol II transcription units, 3' end
formation and transcription termination are mandatory steps in mRNA
biosynthesis and in the definition of the transcription unit. As we are
defining gene regulation by 3' end processing, we are necessarily also
considering how 3' end processing affects i.) pol II transcription
termination ii.) splice site recognition and utilization and iii.)
transport of mRNA from the nucleus to the cytoplasm. Each of these steps
is recognized as playing an increasingly large role in the strategy of
eucaryotic gene regulation.
The specific goal of this research plan is to extend our characterization
of the molecular biology and biochemistry of 3' end formation and
transcription termination in RNA pol II transcription units. We are
characterizing regulation of poly(A) site use in tandem poly(A) site
containing transcription units to understand how poly(A) site choice is
determined for complex transcription units. These studies necessarily
require a comparison to function of individual poly(A) sites. The
efficiency of 3' processing for a given substrate pre-mRNA is a major
focus of these studies since it is a key determinant in alternative
processing as well as in transcription termination.
We have shown that recognition and presumably cleavage efficiency at the
poly(A) site is a required first step in formation of a "termination
competent" RNA polymerase II elongation complex. We are extending our
characterization of 3' processing to a characterization of how 3'
processing causes formation of the termination competent elongation
complex.
We are pursuing two parallel and complementing strategies for
characterization of 3' processing and transcription termination; i. in
vivo studies which we are using to identify functional parameters which
are operating to regulate 3' processing and termination within the cell
ii. in vitro studies defining the biochemistry of 3'processing and
transcription termination.
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Sequence-mediated regulation of adenovirus gene expression by repression of mRNA accumulation.
通过抑制 mRNA 积累来序列介导的腺病毒基因表达调控。
DOI:
10.1128/mcb.17.4.2207
发表时间:
1997
期刊:
Molecular and cellular biology
影响因子:
5.3
作者:
[Prescott,JC, Liu,L, Falck-Pedersen,E]
通讯作者:
Falck-Pedersen,E
3' RNA processing efficiency plays a primary role in generating termination-competent RNA polymerase II elongation complexes.
3 RNA 加工效率在生成具有终止能力的 RNA 聚合酶 II 延伸复合物中起主要作用。
DOI:
10.1128/mcb.13.6.3472-3480.1993
发表时间:
1993
期刊:
Molecular and cellular biology
影响因子:
5.3
作者:
[Edwalds-Gilbert,G, Prescott,J, Falck-Pedersen,E]
通讯作者:
Falck-Pedersen,E
Varied poly(A) site efficiency in the adenovirus major late transcription unit.
腺病毒主要晚期转录单位中不同的聚腺苷酸位点效率。
DOI:
--
发表时间:
1992
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Prescott,JC, Falck-Pedersen,E]
通讯作者:
Falck-Pedersen,E
Sequences regulating temporal poly(A) site switching in the adenovirus major late transcription unit.
调节腺病毒主要晚期转录单位中时间性 Poly(A) 位点转换的序列。
DOI:
10.1128/mcb.11.12.5977-5984.1991
发表时间:
1991
期刊:
Molecular and cellular biology
影响因子:
5.3
作者:
[DeZazzo,JD, Falck-Pedersen,E, Imperiale,MJ]
通讯作者:
Imperiale,MJ
Thyrotropin-releasing hormone (TRH) receptor number determines the size of the TRH-responsive phosphoinositide pool. Demonstration using controlled expression of TRH receptors by adenovirus mediated gene transfer.
促甲状腺激素释放激素 (TRH) 受体的数量决定了 TRH 反应性磷酸肌醇库的大小。
DOI:
--
发表时间:
1994
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Gershengorn,MC, Heinflink,M, Nussenzveig,DR, Hinkle,PM, Falck-Pedersen,E]
通讯作者:
Falck-Pedersen,E
共 8 条
Regulation of host cell inflammatory and maturation response through AdV DNAdete
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批准号:8286154
-
项目类别:
-
资助金额:$42.25万
-
财政年份:2011
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Regulation of host cell inflammatory and maturation response through AdV DNAdete
-
批准号:8686730
-
项目类别:
-
资助金额:$42.25万
-
财政年份:2011
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Regulation of host cell inflammatory and maturation response through AdV DNAdete
-
批准号:8477123
-
项目类别:
-
资助金额:$39.72万
-
财政年份:2011
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Regulation of host cell inflammatory and maturation response through AdV DNAdete
-
批准号:8084949
-
项目类别:
-
资助金额:$42.25万
-
财政年份:2011
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Ad5 Fiber and Penton mts: Influence on immune activation
-
批准号:7146705
-
项目类别:
-
资助金额:$39.82万
-
财政年份:2004
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Ad5 Fiber and Penton mts: Influence on immune activation
-
批准号:6986149
-
项目类别:
-
资助金额:$41.01万
-
财政年份:2004
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Adenovirus Activation of Antigen Presenting Cells Through DNA Sensing Mechanisms
-
批准号:8105569
-
项目类别:
-
资助金额:$50.78万
-
财政年份:2004
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Ad5 Fiber and Penton mts: Influence on immune activation
-
批准号:6857191
-
项目类别:
-
资助金额:$42.0万
-
财政年份:2004
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Ad5 Fiber and Penton mts: Influence on immune activation
-
批准号:7318336
-
项目类别:
-
资助金额:$39.07万
-
财政年份:2004
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
Ad5 Fiber and Penton mts: Influence on immune activation
-
批准号:7534981
-
项目类别:
-
资助金额:$39.07万
-
财政年份:2004
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
AAV p51EE Rep mediated integration into Chr19 AAVS1 site
-
批准号:6766724
-
项目类别:
-
资助金额:$29.66万
-
财政年份:2003
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
AAV p51EE Rep mediated integration into Chr19 AAVS1 site
-
批准号:6927945
-
项目类别:
-
资助金额:$29.66万
-
财政年份:2003
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
AAV p51EE Rep mediated integration into Chr19 AAVS1 site
-
批准号:7104197
-
项目类别:
-
资助金额:$28.97万
-
财政年份:2003
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
AAV p51EE Rep mediated integration into Chr19 AAVS1 site
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批准号:6681351
-
项目类别:
-
资助金额:$29.66万
-
财政年份:2003
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
GENE MODIFICATION OF ADENOVIRUS CAPSID PROTEINS
-
批准号:6318390
-
项目类别:
-
资助金额:$25.26万
-
财政年份:2000
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
GENE MODIFICATION OF ADENOVIRUS CAPSID PROTEINS
-
批准号:6110289
-
项目类别:
-
资助金额:$25.26万
-
财政年份:1999
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
CORE--MOLECULAR BIOLOGY
-
批准号:6242297
-
项目类别:
-
资助金额:$9.04万
-
财政年份:1997
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
MODIFICATION OF THE ADENOVIRUS FIBER TO ALTER THE TARGET RECEPTOR SPECIFICITY
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批准号:6242296
-
项目类别:
-
资助金额:$9.04万
-
财政年份:1997
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
RNA POL II POLY-A SITE AND 3' TERMINATION
-
批准号:2181161
-
项目类别:
-
资助金额:$28.38万
-
财政年份:1990
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
RNA POL II POLY-A SITE AND 3' TERMINATION
-
批准号:2181162
-
项目类别:
-
资助金额:$29.95万
-
财政年份:1990
-
负责人:ERIK S FALCK-PEDERSEN
-
依托单位:
海外基金