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Sequence variation in the human transcription factor gene POU5F1.

Sequence variation in the human transcription factor gene POU5F1. Research Abstract Details 

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  • Sequence variation in the human transcription factor gene POU5F1. Abstract Text:

    shehnaz k hussainShehnaz K Hussain,reynaldo sequerraReynaldo Sequerra,caterina bertucciCaterina Bertucci,noel c hastingsNoel C Hastings,mark riederMark Rieder,stephen m schwartzStephen M Schwartz,shehnaz k hussainShehnaz K Hussain,reynaldo sequerraReynaldo Sequerra,caterina bertucciCaterina Bertucci,noel c hastingsNoel C Hastings,mark riederMark Rieder,stephen m schwartzStephen M Schwartz,

    BACKGROUND: POU5F1 expression is required to maintain stem cell pluripotency and for primordial germ cells to retain proliferative capability in embryonic development. Recent evidence suggests that POU5F1 may also be a testicular germ cell carcinoma (TGCC) oncogene, and POU5F1 variation may influence TGCC risk. As an important first step to a genetic association study, we sought to identify all common sequence variants in an 11.3 kb region containing POU5F1, and to describe the linkage disequilibrium patterns, using DNA from individuals of African-descent (AD) and European-descent (ED). RESULTS: A higher number of polymorphisms was observed in the AD (n = 102) versus ED (n = 82) population. Among the 41 observed haplotypes, 21 (51%) and 12 (29%) were unique to the AD and ED populations, respectively, while 8 (20%) were observed in both. The number of tagging polymorphisms necessary to explain at least 80% of common variation (minor allele frequency > or = 0.10) due to the remaining untyped polymorphisms was 17 for an AD and 10 for an ED population, providing a 4.0- and 7.0-fold gain in genotyping efficiency for characterizing nucleotide variation, respectively. CONCLUSION: POU5F1 is highly polymorphic, however a smaller subset of polymorphisms can tag the observed genetic variation with little loss of information.

    Sequence variation in the human transcription factor gene POU5F1. Publishing Authors By Initials

    sk hussainSK Hussain,r sequerraR Sequerra,c bertucciC Bertucci,nc hastingsNC Hastings,m riederM Rieder,sm schwartzSM Schwartz,sk hussainSK Hussain,r sequerraR Sequerra,c bertucciC Bertucci,nc hastingsNC Hastings,m riederM Rieder,sm schwartzSM Schwartz,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

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    Sequence variation in the human transcription factor gene POU5F1. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: BMC genetics

    VOLUME: 9

    Page Numbers: 15

    Journal Abbreviation: BMC Genet.

    ISSN: 1471-2156

    DAY: 6

    MONTH: 02

    YEAR: 2008

    Sequence variation in the human transcription factor gene POU5F1. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100966978

    Sequence variation in the human transcription factor gene POU5F1. Keywords Mesh Terms:

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    Grant and Affiliation Information for Sequence variation in the human transcription factor gene POU5F1.

    AFFILIATION: University of California, Los Angeles, Division of Cancer Prevention and Control Research, School of Public Health and Jonsson Comprehensive Cancer Center, Los Angeles, CA, 90095-6900, USA. SKHussain@ucla.edu

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NCI

    GRANT: R25CA094880

    ACRONYM: CA

    MEDLINETA: BMC Genet

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