MOLECULAR GENETICS OF DOSAGE COMPENSATION IN DROSOPHILA
MOLECULAR GENETICS OF DOSAGE COMPENSATION IN DROSOPHILA
批准号:
2183361
负责人:
Mitzi I Kuroda
金额:
$8.03万
依托单位国家:
美国
项目类别:
财政年份:
1991
资助国家:
美国
项目状态:
已结题
起止时间:
1991-04-01 至 1996-03-31
关键词:
Drosophilidae SDS polyacrylamide gel electrophoresis adenosinetriphosphatase affinity chromatography binding proteins chemical binding complementary DNA fluorescence microscopy gender difference gene dosage gene expression genetic mapping genetic regulatory element helicase immunological substance laboratory rabbit molecular cloning molecular genetics nucleic acid sequence phosphorylation polymerase chain reaction protein sequence regulatory gene scintillation counter sex chromosomes
中文摘要
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英文摘要
X chromosome gene expression is equalized in males and females
in a process called dosage compensation. In Drosophila, dosage
compensation occurs by increased transcription of X-linked genes in
males and is essential for male viability. The product of the
maleless (mle) gene is required in males for dosage compensation to
occur. The mle protein (Mle) is associated with hundreds of sites
on the X chromosome in the male, making it a strong candidate to
directly regulate X chromosome transcription.
The long term objective of this work is to understand the
molecular mechanism of dosage compensation in Drosophila . The
experiments proposed focus on the Mle protein. Specific goals are:
I. To complete the analysis of mle gene structure and protein
expression pattern. II. To define the biochemical activity of Mle
protein. III. To characterize X chromosome binding sites of Mle.
IV. To determine whether other genes in the dosage compensation
genetic hierarchy regulate male-specific activity of Mle. V. To
extend these studies toward a more complete understanding of dosage
compensation by cloning additional regulatory genes.
The amino acid sequence of Mle contains short motifs which
place it in a superfamily of ATP binding proteins that are known or
putative helicases. The hypothesis that He is a helicase will be
tested indirectly, by measuring ATPase activity in the presence of
nucleic acids, and directly, by unwinding assays of synthetic
duplexes of DNA, RNA and DNA/RNA hybrids. Chromosome binding
experiments will map the segments of specific X-linked genes that
Mle associates with in vivo.
Although Mle is active in males and not in females, Me protein
is present in both sexes. The effect of other dosage compensation
mutants on Me activity will be tested. X chromosome binding by Me,
and any biochemical activities of He that are discovered will be
assayed in Sxl, msl-1, msl-2, and mle-3 mutants. An understanding
of how dosage compensation occurs may require isolation of the other
known regulatory genes and characterization of their products.
Isolation of msl-2 will proceed using standard methods for cloning
Drosophila genes.
It is well documented, especially in Drosophila and humans,
that chromosomal balance is necessary for normal development.
Mechanisms to equalize X-linked gene expression in males and females
exist in many organisms, and disruption of these systems can
severely affect development and viability. An understanding of how
dosage compensation occurs in Drosophila may have relevance to
general mechanisms of chromatin organization and coordinate gene
regulation during development.
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资助金额:$71.76万
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财政年份:2018
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Epigenetic regulation of transcriptional programming
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资助金额:$71.76万
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财政年份:2018
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Comprehensive analysis of epigenetic regulators in their native chromatin context
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资助金额:$33.74万
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财政年份:2012
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Comprehensive analysis of epigenetic regulators in their native chromatin context
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资助金额:$33.74万
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财政年份:2012
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Comprehensive analysis of epigenetic regulators in their native chromatin context
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批准号:9037141
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资助金额:$36.92万
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财政年份:2012
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依托单位:
Comprehensive analysis of epigenetic regulators in their native chromatin context
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批准号:8788710
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项目类别:
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资助金额:$33.74万
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财政年份:2012
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负责人:Mitzi I Kuroda
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依托单位:
Comprehensive analysis of epigenetic regulators in their native chromatin context
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批准号:8459396
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项目类别:
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资助金额:$32.56万
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财政年份:2012
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负责人:Mitzi I Kuroda
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依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
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批准号:7901767
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项目类别:
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资助金额:$26.46万
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财政年份:2009
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负责人:Mitzi I Kuroda
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依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
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批准号:6401873
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项目类别:
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资助金额:$3.76万
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财政年份:2001
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负责人:Mitzi I Kuroda
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依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
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批准号:6530113
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项目类别:
-
资助金额:$4.1万
-
财政年份:2001
-
负责人:Mitzi I Kuroda
-
依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
-
批准号:6834386
-
项目类别:
-
资助金额:$4.1万
-
财政年份:2001
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负责人:Mitzi I Kuroda
-
依托单位:
MOLECULAR GENETICS OF DOSAGE COMPENSATION IN DROSOPHILA
-
批准号:2392138
-
项目类别:
-
资助金额:$9.56万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位:
MOLECULAR GENETICS OF DOSAGE COMPENSATION IN DROSOPHILA
-
批准号:6386169
-
项目类别:
-
资助金额:$13.94万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位:
MOLECULAR GENETICS OF DOSAGE COMPENSATION IN DROSOPHILA
-
批准号:6636025
-
项目类别:
-
资助金额:$13.94万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
-
批准号:8052824
-
项目类别:
-
资助金额:$43.68万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
-
批准号:8245208
-
项目类别:
-
资助金额:$43.74万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
-
批准号:7784437
-
项目类别:
-
资助金额:$44.06万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位:
MOLECULAR GENETICS OF DOSAGE COMPENSATION IN DROSOPHILA
-
批准号:2900748
-
项目类别:
-
资助金额:$13.33万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位:
Molecular Genetics of Dosage Compensation in Drosophila
-
批准号:8448216
-
项目类别:
-
资助金额:$42.21万
-
财政年份:1991
-
负责人:Mitzi I Kuroda
-
依托单位: