A Transcript Map for the 2.8-Mb Region Containing the Multiple Endocrine Neoplasia Type 1 Locus
Autor: | Lance A. Liotta, Francis S. Collins, Burns Lee, Bruce A. Roe, Settara C. Chandrasekharappa, Pachiappan Manickam, Siradanahalli C. Guru, Yingping Wang, Shodimu Emmanuel Olufemi, Allen M. Spiegel, Jane M. Weisemann, Sunita K. Agarwal, Young Sik Kim, Mark S. Boguski, Michael R. Emmert-Buck, Stephen J. Marx, Mary Beth Kester, Judy S. Crabtree |
---|---|
Rok vydání: | 1997 |
Předmět: |
Genetics
Transcription Genetic Tumor suppressor gene Genetic Linkage Genome Human Chromosomes Human Pair 11 Molecular Sequence Data Chromosome Mapping Locus (genetics) Biology medicine.disease Molecular biology Paraspeckles Loss of heterozygosity Multiple Endocrine Neoplasia Type 1 Mutation testing medicine Humans MEN1 Letters Multiple endocrine neoplasia Gene Genetics (clinical) |
Zdroj: | Genome Research. 7:725-735 |
ISSN: | 1549-5469 1088-9051 |
DOI: | 10.1101/gr.7.7.725 |
Popis: | Multiple endocrine neoplasia type 1 (MEN 1) is an inherited cancer syndrome in which affected individuals develop multiple parathyroid, enteropancreatic, and pituitary tumors. The locus for MEN1 is tightly linked to the marker PYGM on chromosome 11q13, and linkage analysis places the MEN1 gene within a 2-Mb interval flanked by the markers D11S1883 and D11S449. Loss of heterozygosity studies in MEN 1 and sporadic tumors suggest that theMEN1 gene encodes a tumor suppressor and have helped to narrow the location of the gene to a 600-kb interval between PYGM andD11S449. Focusing on this smaller MEN1 interval, we have identified and mapped 12 transcripts to this 600-kb region. A precise ordered map of 33 transcripts, including 12 genes known to map to this region, was generated for the 2.8-Mb D11S480–D11S913interval. Fifteen candidate genes (of which 10 were examined exhaustively) were evaluated by Southern blot and/or dideoxy fingerprinting analysis to identify the gene harboring disease-causing mutations.[The sequence data described in this paper have been submitted to GenBank under accession nos. EST06996, U93236,AF001540–AF001547, AF001433–AF001436, AF001891–AF001893,N55476, R19205, and W37647 (see Table 1 for listing of transcripts). The BAC clone sequences have been submitted to GenBank under accession nos. AC000134, AC000159, and AC000353.] |
Databáze: | OpenAIRE |
Externí odkaz: |