LOCALIZATION OF THE WILMS TUMOR SUSCEPTIBILITY GENE(S)
LOCALIZATION OF THE WILMS TUMOR SUSCEPTIBILITY GENE(S)
批准号:
2194397
负责人:
STANLEY F. NELSON
金额:
$8.56万
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:
1991-05-01 至 1996-04-30
关键词:
Wilms' tumor artificial chromosomes chromosome walking gene expression genetic library genetic manipulation genetic mapping genetic transcription human genetic material tag molecular cloning neoplasm /cancer immunology neoplastic cell northern blottings nucleic acid probes nucleic acid sequence pulsed field gel electrophoresis tumor suppressor genes
中文摘要
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英文摘要
Wilm's tumor is one of the most common malignancies of children.
Strong evidence indicates that tumor suppressor genes are located
at 11p13 and 11p15.5. Deletions in these regions contribute to
the genesis of Wilm's tumor. To understand the basic defect in
this cancer, the Wilms tumor genes (WTG) at 11p13 and 11p15.5 must
be isolated and their products analyzed. To this end, an
overlapping library of human chromosome 11 will be made in yeast
artificial chromosome (YAC) vectors using DNA from a human:rodent
hybrid cell line. Insert DNA will be partially digested and size
selected >400kb. The YAC library will be screened with known
probes from the 11p13 and 11p15.5 regions. Comprehensive
overlapping libraries of the 1500kb of 11p13 and the 20mb of
11p15.5 will be created. The YAC inserts will be compared to
existing maps of the regions. YAC chromosome walking will be used
to fill in gaps between known probes. Any gaps that are not able
to be cloned in YACs will be cloned in cosmid or lambda vectors.
The regions will be physically mapped with pulsed field gel
electrophoresis capable of resolving 50-5000kb fragments of DNA.
Panels of DNA from Wilm's tumors will be used to more precisely map
the WTG locus in 11p15.5. Transcribed regions of the 11p13 and
11p15.5 libraries will be isolated by several methods: 1)
insertional mutagenesis with a selectable marker; 2) hybridization
with cDNA from human kidney; 3) identification of unmethylated CpG
islands; and 4) cross-species hybridization. Probes that detect
expressed genes will be hybridized to Northern blots of mRNA from
multiple Wilm's tumors. Probes that detect variable sizes or
decreased levels mRNA from some of the Wilm's tumors will be
candidate WTG exon probes. Additionally, the YACs will be tested
for tumor suppression function by spheroplast fusion into a Wilm's
tumor cell line, G401. If a YAC clone is able to suppress
tumorigenicity, deletion analysis and insertional mutagenesis would
greatly facilitate localization of a WTG.
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