MOLECULAR BIOLOGY OF OSTEOARTHRITIS & CHONDRODYSPLASIAS
MOLECULAR BIOLOGY OF OSTEOARTHRITIS & CHONDRODYSPLASIAS
批准号:
2077362
负责人:
PAUL L KATZENSTEIN
金额:
$9.01万
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:
1991-09-18 至 1995-08-31
关键词:
achondroplasia alleles articular cartilage cartilage development cartilage disorder cartilage metabolism collagen disease /disorder model electron microscopy endonuclease gene expression gene mutation genetic manipulation genetically modified animals immunoelectron microscopy in situ hybridization laboratory mouse model design /development molecular cloning northern blottings nucleic acid sequence osteoarthritis phenotype polymerase chain reaction protein structure function proteoglycan radiography restriction mapping tissue /cell culture
中文摘要
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英文摘要
This Physician Scientist Award proposal is designed to permit the candidate
to acquire basic and advanced knowledge and skills in molecular biologic
investigation and to apply these to the study of cartilage diseases.
Graduate coursework in cell and molecular biology and protein biochemistry
which provide a firm basis for future research endeavors will be taken
during the first year of this Award.
During Phase I, transgenic mouse models of human disease, containing
mutations in the alpha2 chain of type IX collagen, will be generated. Type
IX collagen Is a cartilage-specific molecule with unique structural
features that likely render the molecule necessary for normal cartilage
structure and function. Because mutations in type II collagen have been
shown to cause human disease, it is quite likely that abnormalities of type
IX collagen do also. Three or four mutations in the alpha2 (IX) chain,
which contains interchain disulfide bridges, crosslink sites to type II
collagen, a glycosaminoglycan attachment site and a kink region, will be
constructed and transgenic mice containing these mutations generated.
Abnormal phenotypes will be characterized radiographically and
microscopically.
During Phase II, mechanisms by which these mutations alter normal
development, structure and function of cartilage will be sought. At the
same time, information on the structure-function relationship of various
domains of the type IX molecule will be obtained. This phase of the Award
will prepare the candidate for additional studies of the molecular genetics
of human cartilage diseases.
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