GENETIC AND MOLECULAR BASIS OF FAMILIAL COLD URTICARIA
GENETIC AND MOLECULAR BASIS OF FAMILIAL COLD URTICARIA
批准号:
6137079
负责人:
HAROLD M HOFFMAN
金额:
$11.72万
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 2002-12-31
关键词:
autosomal dominant trait chromosome walking clinical research cold temperature family genetics gene expression gene rearrangement genetic mapping genetic polymorphism human subject inflammation linkage mapping molecular biology molecular cloning molecular genetics pulsed field gel electrophoresis sequence tagged sites single strand conformation polymorphism urticaria
中文摘要
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英文摘要
The long term objective of this project is the localization and
identification of the gene responsible for familial cold urticaria.
Familial cold urticaria is an excellent example of the immune system's
response to physical stimuli in the environment. This condition
provides a novel opportunity to study underlying mechanisms of
inflammation from a molecular genetic perspective because of its
classical autosomal dominant inheritance pattern. It is unique to have
a large affected family motivated to participate in the proposed
research in close proximity to UCSD which has the resources necessary
to perform molecular genetic studies. There are many inflammatory
diseases induced by physical stimuli and they may share common
mechanisms with other inflammatory disorders. Therefore this genetic
study of familial cold urticaria will likely increase the understanding
of the molecular mechanisms regulating inflammatory responses.
Ultimately this will lead to improved treatment of familial cold
urticaria and other inflammatory disorders.
The specific goals of this project are: (1) to conduct a systematic
survey of the entire genome using short tandem repeat polymorphisms with
markers spaced at 20 centiMorgans (cM) initially and later at 10 cM if
necessary; (2) to perform multi-point linkage analysis using the LINKAGE
program to identify regions with a lod score greater than plus 2 and
after finer mapping of these regions to identify regions with a lod
score greater than plus 3 and an approximate size of 1-2 cM; (3) to
develop a contiguous physical map using a combination of cloning systems
and techniques such as chromosome walking and STS content mapping; (4)
to identify candidate genes within the limited region using techniques
such as cDNA selection and exon trapping; and (5) to screen these genes
initially for gross rearrangements using pulse field gel electrophoresis
and then for more subtle DNA alterations using single strand
conformational polymorphism analysis. The achievement of these goals
will result in identification of the gene responsible for familial cold
urticaria which will ultimately lead to an understanding of the
mechanism of the inflammatory response to a physical stimulus.
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依托单位:
海外基金