ISOLATION OF THE GENE FOR CHEDIAK-HIGASHI SYNDROME
ISOLATION OF THE GENE FOR CHEDIAK-HIGASHI SYNDROME
批准号:
3082899
负责人:
RANDALL F HOLCOMBE
金额:
$6.03万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-09-01 至 1994-08-31
关键词:
Chediak Higashi syndrome T lymphocyte biological polymorphism complementary DNA cytogenetics disease /disorder model gel electrophoresis gene expression gene therapy genetic disorder genetic disorder diagnosis genetic library genetic manipulation genetic mapping genetic markers genetic transcription homeostasis human tissue immunodeficiency laboratory mouse linkage mapping molecular cloning nucleic acid hybridization nucleic acid probes population genetics prenatal diagnosis
中文摘要
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英文摘要
Chediak-Higashi syndrome (CHS) is a rare immuno-deficiency disease with
manifestations involving alterred hemostasis, an increase in the frequency
of malignancies, abnormal function of lysosomes with resultant lack of
"Natural Killer" activity, and an increase in a specific subset of
T-lymphocytes. The gene responsible for the syndrome has not been
characterized in either the human or murine system, although the
chromosomal location of the gene causing the analogous syndrome in mice
(bg) has been identified.
The goals of this project are: 1) Generate a murine "jumping library" to
identify new probes close to bg, 2) Define restriction fragment length
polymorphisms (RFLP) with these probes through cross hybridization with
human DNA, 3) Determine genetic linkage of the probes to the CHS gene by
RFLP and family analysis, 4) analyze human and murine northern blots to
identify transcripts of the putative gene and 5) sequence putative CHS
genes and predict the protein product.
The technology for identifying a gene by "reverse genetics" on the basis of
its chromosomal location exists and should be facilitated in this instance
by the presence of an animal model for which the gene has been previously
mapped. Identification of the CHS gene should provide information about
hemostasis, immune surveillance, lysosomal function, and the in vivo
function of gamma delta T-lymphocytes.
Dr. Randall Holcombe is completing training in the medical subspecialties
of hematology and oncology and has already initiated a productive research
program concerning CHS. He has developed expertise in the molecular
biological techniques required for the successful completion of the
research program described herein over the prior two years. The Department
of Genetics, where the bulk of the research will be performed, has the
equipment necessary for recombinant DNA research, with tissue culture and
animal facilities. The Hematology Division and the Department of Genetics
sponsor journal clubs, lab meetings, and several lecture series, and
provide an exciting and stimulating environment for research.
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