Functional map of a segment on mouse chromosome 5
Functional map of a segment on mouse chromosome 5
批准号:
6475352
负责人:
MAJA BUCAN
金额:
$38.0万
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:
1991-07-01 至 2007-04-30
关键词:
alleles artificial chromosomes chromosome aberrations chromosome deletion chromosome inversion computer assisted sequence analysis developmental genetics gene complementation gene expression gene mutation genetic mapping laboratory mouse molecular cloning molecular genetics nucleic acid hybridization nucleic acid probes nucleic acid sequence pulsed field gel electrophoresis restriction mapping southern blotting
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The elucidation of the functional content
of the genome of a model organism, such as the mouse, involves identification
of genes and evolutionarily conserved non-transcribed sequences through genome
sequencing, analysis of gene expression and analysis of normal and mutant
phenotypes. This grant application is being prepared at an exciting time for
mammalian biology, when each one of these efforts is being undertaken on a
large scale - whole genome level. In this project we propose to initiate the
integration of these functional genomics data, using a 100 Mb chromosomal
region of the mouse genome as a model. Our aims are to (1) identify,
characterize and clone a set of novel embryo-lethal mutations within the
30cM/60 Mb region covered by the Rw inversion (2) perform functional analysis
of the cluster of GABAA receptor subunit genes by generation of Embryonic Stem
(ES) cells with chromosomal deletions and phenotypic analysis of mice carrying
these deletions and (3) assemble a gene index and perform comparative sequence
analysis of genes shown to be involved in developmental processes (based on
mutant analysis and/or available expression data). The minimal set of genes
necessary for embryonic survival is a key question in developmental biology. In
this proposal we use a defined chromosomal region, representing 2 percent of
the mouse genome, and available genetic, genomic and bioinformatics resources
to systematically search for and catalog these genes and their mutant
phenotypes.
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