| Literature DB >> 11935316 |
Ester Rozenblum1, Pia Vahteristo, Therese Sandberg, Jon Thor Bergthorsson, Kirsi Syrjakoski, Don Weaver, Karin Haraldsson, Hrefna Kristin Johannsdottir, Paula Vehmanen, Savita Nigam, Natalie Golberger, Christiane Robbins, Evgenia Pak, Amalia Dutra, Elizabeth Gillander, Dietrich A Stephan, Joan Bailey-Wilson, Suh-Hang Hank Juo, Tommi Kainu, Adalgeir Arason, Rosa Bjork Barkardottir, Heli Nevanlinna, Ake Borg, Olli-P Kallioniemi.
Abstract
Chromosomal region 13q21-q22 harbors a putative breast cancer susceptibility gene and has been implicated as a common site for somatic deletions in a variety of malignant tumors. We have built a complete physical clone contig for a region between D13S1308 and AFM220YE9 based on 18 yeast artificial chromosome and 81 bacterial artificial chromosome (BAC) clones linked together by 22 genetic markers and 61 other sequence tagged sites. Combining data from 47 sequenced BACs (as of June 2001), we have assembled in silico an integrated 5.7-Mb genomic map with 90% sequence coverage. This area contains eight known genes, two hypothetical proteins, 24 additional Unigene clusters, and approximately 100 predicted genes and exons. We have determined the cDNA and genomic sequence, and tissue expression profiles for the KIAA1008 protein (homologous to the yeast mitotic control protein dis3+), KLF12 (AP-2 repressor), progesterone induced blocking factor 1, zinc finger transcription factor KLF5, and LIM domain only-7, and for the hypothetical proteins FLJ22624 and FLJ21869. Mutation screening of the five known genes in 19 breast cancer families has revealed numerous polymorphisms, but no deleterious mutations. These data provide a basis and resources for further analyses of this chromosomal region in the development of cancer.Entities:
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Year: 2001 PMID: 11935316 DOI: 10.1007/s00439-001-0646-6
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132