Literature DB >> 17353897

Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis.

Lekbir Baala1, Sylvain Briault, Heather C Etchevers, Frédéric Laumonnier, Abdelhafid Natiq, Jeanne Amiel, Nathalie Boddaert, Capucine Picard, Aziza Sbiti, Abdellah Asermouh, Tania Attié-Bitach, Féréchté Encha-Razavi, Arnold Munnich, Abdelaziz Sefiani, Stanislas Lyonnet.   

Abstract

Neural progenitor proliferation and migration influence brain size during neurogenesis. We report an autosomal recessive microcephaly syndrome cosegregating with a homozygous balanced translocation between chromosomes 3p and 10q, and we show that a position effect at the breakpoint on chromosome 3 silences the eomesodermin transcript (EOMES), also known as T-box-brain2 (TBR2). Together with the expression pattern of EOMES in the developing human brain, our data suggest that EOMES is involved in neuronal division and/or migration. Thus, mutations in genes encoding not only mitotic and apoptotic proteins but also transcription factors may be responsible for malformative microcephaly syndromes.

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Year:  2007        PMID: 17353897     DOI: 10.1038/ng1993

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  80 in total

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3.  Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway.

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4.  Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria.

Authors:  Mary C O'Driscoll; Sarah B Daly; Jill E Urquhart; Graeme C M Black; Daniela T Pilz; Knut Brockmann; Meriel McEntagart; Ghada Abdel-Salam; Maha Zaki; Nicole I Wolf; Roger L Ladda; Susan Sell; Stefano D'Arrigo; Waney Squier; William B Dobyns; John H Livingston; Yanick J Crow
Journal:  Am J Hum Genet       Date:  2010-08-19       Impact factor: 11.025

5.  Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.

Authors:  William B Dobyns; Ghayda Mirzaa; Susan L Christian; Kristin Petras; Jessica Roseberry; Gary D Clark; Cynthia J R Curry; Donna McDonald-McGinn; Livija Medne; Elaine Zackai; Julie Parsons; Dina J Zand; Fuki M Hisama; Christopher A Walsh; Richard J Leventer; Christa L Martin; Marzena Gajecka; Lisa G Shaffer
Journal:  Am J Med Genet A       Date:  2008-07-01       Impact factor: 2.802

Review 6.  Common themes emerge in the transcriptional control of T helper and developmental cell fate decisions regulated by the T-box, GATA and ROR families.

Authors:  Sara A Miller; Amy S Weinmann
Journal:  Immunology       Date:  2009-03       Impact factor: 7.397

7.  A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations.

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Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-26       Impact factor: 11.205

8.  T-bet's ability to regulate individual target genes requires the conserved T-box domain to recruit histone methyltransferase activity and a separate family member-specific transactivation domain.

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Journal:  Mol Cell Biol       Date:  2007-10-08       Impact factor: 4.272

9.  Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition.

Authors:  Catherine A Brownstein; Meghan C Towne; Lovelace J Luquette; David J Harris; Nicholas S Marinakis; Peter Meinecke; Kerstin Kutsche; Philippe M Campeau; Timothy W Yu; David M Margulies; Pankaj B Agrawal; Alan H Beggs
Journal:  Eur J Med Genet       Date:  2013-10-28       Impact factor: 2.708

10.  Reduced cortical surface area in adolescents with conduct disorder.

Authors:  Sagari Sarkar; Eileen Daly; Yue Feng; Christine Ecker; Michael C Craig; Duncan Harding; Quinton Deeley; Declan G M Murphy
Journal:  Eur Child Adolesc Psychiatry       Date:  2014-12-07       Impact factor: 4.785

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