Literature DB >> 7959731

Human brain factor 1, a new member of the fork head gene family.

D B Murphy1, S Wiese, P Burfeind, D Schmundt, M G Mattei, W Schulz-Schaeffer, U Thies.   

Abstract

Analysis of cDNA clones that cross-hybridized with the fork head domain of the rat HNF-3 gene family revealed 10 cDNAs from human fetal brain and human testis cDNA libraries containing this highly conserved DNA-binding domain. Three of these cDNAs (HFK1, HFK2, and HFK3) were further analyzed. The cDNA HFK1 has a length of 2557 nucleotides and shows strong homology at the nucleotide level (91.2%) to brain factor 1 (BF-1) from rat. The HFK1 cDNA codes for a putative 476 amino acid protein. The homology to BF-1 from rat in the coding region at the amino acid level is 87.5%. The fork head homologous region includes 111 amino acids starting at amino acid 160 and has a 97.5% homology to BF-1. Southern hybridization revealed that HFK1 is highly conserved among mammalian species and possibly birds. Northern analysis with total RNA from human tissues and poly(A)-rich RNA from mouse revealed a 3.2-kb transcript that is present in human and mouse fetal brain and in adult mouse brain. In situ hybridization with sections of mouse embryo and human fetal brain reveals that HFK1 expression is restricted to the neuronal cells in the telencephalon, with strong expression being observed in the developing dentate gyrus and hippocampus. HFK1 was chromosomally localized by in situ hybridization to 14q12. The cDNA clones HFK2 and HFK3 were analyzed by restriction analysis and sequencing. HFK2 and HFK3 were found to be closely related but different from HFK1. Therefore, it would appear that HFK1, HFK2, HFK3, and BF-1 form a new fork head related subfamily.

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Year:  1994        PMID: 7959731     DOI: 10.1006/geno.1994.1313

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  25 in total

1.  DNA microarray analysis of functionally discrete human brain regions reveals divergent transcriptional profiles.

Authors:  S J Evans; P V Choudary; M P Vawter; J Li; J H Meador-Woodruff; J F Lopez; S M Burke; R C Thompson; R M Myers; E G Jones; W E Bunney; S J Watson; H Akil
Journal:  Neurobiol Dis       Date:  2003-11       Impact factor: 5.996

2.  Transducin-like enhancer of Split-1 (TLE1) combines with Forkhead box protein G1 (FoxG1) to promote neuronal survival.

Authors:  Somasish Ghosh Dastidar; Sriram Narayanan; Stefano Stifani; Santosh R D'Mello
Journal:  J Biol Chem       Date:  2012-02-21       Impact factor: 5.157

3.  Gene expression profile in bone of diabetes-prone BB/OK rats fed a high-fat diet.

Authors:  Jörn Lange; Thomas Barz; Axel Ekkernkamp; Ingrid Klöting; Niels Follak
Journal:  Genes Nutr       Date:  2012-05-26       Impact factor: 5.523

4.  FoxG1 and TLE2 act cooperatively to regulate ventral telencephalon formation.

Authors:  Martin Roth; Boyan Bonev; Jennefer Lindsay; Robert Lea; Niki Panagiotaki; Corinne Houart; Nancy Papalopulu
Journal:  Development       Date:  2010-03-31       Impact factor: 6.868

5.  FoxG1 promotes the survival of postmitotic neurons.

Authors:  Somasish Ghosh Dastidar; Paul Michael Zagala Landrieu; Santosh R D'Mello
Journal:  J Neurosci       Date:  2011-01-12       Impact factor: 6.167

6.  The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.

Authors:  Fanny Kortüm; Soma Das; Max Flindt; Deborah J Morris-Rosendahl; Irina Stefanova; Amy Goldstein; Denise Horn; Eva Klopocki; Gerhard Kluger; Peter Martin; Anita Rauch; Agathe Roumer; Sulagna Saitta; Laurence E Walsh; Dagmar Wieczorek; Gökhan Uyanik; Kerstin Kutsche; William B Dobyns
Journal:  J Med Genet       Date:  2011-03-25       Impact factor: 6.318

7.  Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly.

Authors:  Sarah A Shoichet; Stella-Amrei Kunde; Petra Viertel; Can Schell-Apacik; Hubertus von Voss; Niels Tommerup; Hans-Hilger Ropers; Vera M Kalscheuer
Journal:  Hum Genet       Date:  2005-08-17       Impact factor: 4.132

8.  Primary structure of hepatocyte nuclear factor/forkhead homologue 4 and characterization of gene expression in the developing respiratory and reproductive epithelium.

Authors:  B P Hackett; S L Brody; M Liang; I D Zeitz; L A Bruns; J D Gitlin
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

Review 9.  Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.

Authors:  Francois Dominique Jacob; Vijay Ramaswamy; John Andersen; Francois V Bolduc
Journal:  Eur J Hum Genet       Date:  2009-07-22       Impact factor: 4.246

10.  14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.

Authors:  Carolyn J Ellaway; Gladys Ho; Elisa Bettella; Alisa Knapman; Felicity Collins; Anna Hackett; Fiona McKenzie; Artur Darmanian; Gregory B Peters; Kerry Fagan; John Christodoulou
Journal:  Eur J Hum Genet       Date:  2012-09-12       Impact factor: 4.246

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