DEVELOPMENTAL EFFECTS OF GROWTH DELAY IN FIDGET MICE
DEVELOPMENTAL EFFECTS OF GROWTH DELAY IN FIDGET MICE
批准号:
6489549
负责人:
WAYNE N. FRANKEL
金额:
$29.7万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-01-01 至 2005-12-31
关键词:
autosomal recessive trait cell proliferation chromosome aberrations developmental genetics epitope mapping eye disorder fluorescence microscopy gene expression gene mutation genetic mapping genetically modified animals in situ hybridization laboratory mouse labyrinth molecular cloning neural plate /tube nucleic acid sequence pleiotropism polymerase chain reaction prenatal growth disorder protein protein interaction protein structure function regulatory gene skeletal disorder yeast two hybrid system
中文摘要
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英文摘要
DESCRIPTION (Adapted from investigator's abstract): This is the first
competitive renewal of an RO1 that proposes to characterize the function of a
newly isolated gene that is mutated in fidget mice, and which the PI has named
fidgetin. In the previous funding cycle, the PI identified the gene by
positional cloning as a novel member of a divergent class of proteins, the AAA
group, that share an ATPase domain, and which may function generally in
processes of protein folding and unfolding. Although the gene is widely
expressed, it's loss of function gives rise to a set of remarkably specific
developmental phenotypes whose molecular and cellular underpinnings are
obscure. The current application will investigate these underpinnings by
determining the subcellular location of fidgetin with a lacZ fusion protein
generated by gene targeting, epitope-tagged constructs introduced into culture
cells, and generating antisera to localize the endogenous protein by
immunocytochemistry (Aim 1). Fidgetin-interacting proteins will be identified
in Aim 2 using a yeast two-hybrid screen followed by in vivo expression and
co-immunoprecipitation studies. In Aim 3, careful analyses of fidgetin RNA
expression during embryonic development of normal and various mutant mice will
be carried out in the context of hypotheses that fidgetin is either upstream or
downstream of genes previously shown when mutated to cause defects similar to
fidget. Finally, Aim 4 will attempt to gain insight into possible redundancy
and action of fidget-related genes by expression studies, modifier gene
mapping, and gene targeting.
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