Literature DB >> 16946494

A homeodomain-zinc finger protein, ZFHX4, is expressed in neuronal differentiation manner and suppressed in muscle differentiation manner.

Kazunori Hemmi1, Dongping Ma, Yutaka Miura, Makoto Kawaguchi, Masakiyo Sasahara, Tomoko Hashimoto-Tamaoki, Taiki Tamaoki, Nobuo Sakata, Kayoko Tsuchiya.   

Abstract

Human ZFHX4 has recently been shown to be a candidate gene for congenital bilateral isolated ptosis. Here, we report molecular cloning of the human ZFHX4 cDNA and genomic organization of this gene. Human ZFHX4 is about 180 kb long, containing 12 exons that encodes a 3599-amino acid protein carrying four homeodomains and 22 zinc fingers. The 11th exon is 3.2 kb in length and encodes all the four homeodomains together with four of the 22 zinc fingers. ZFHX4 is 90% homologous to mouse Zfhx4, 52% to human ATBF1A and 24% to Drosophila ZFH-2. ZFHX4 was mapped to human chromosome 8q13.3-q21.11 by fluorescence in situ hybridization using BAC clone RP11-48D4 as a probe. RT-PCR analysis showed that ZFHX4 transcripts were expressed in adult human brain, liver and muscle. This, together with the finding that Zfhx4 was expressed transiently in differentiating P19 embryonal carcinoma cells and C2C12 myoblasts, suggests that ZFHX4/Zfhx4 is involved in neural and muscle differentiation.

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Year:  2006        PMID: 16946494     DOI: 10.1248/bpb.29.1830

Source DB:  PubMed          Journal:  Biol Pharm Bull        ISSN: 0918-6158            Impact factor:   2.233


  19 in total

1.  Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects.

Authors:  Kazutoyo Osoegawa; David M Iovannisci; Bin Lin; Christina Parodi; Kathleen Schultz; Gary M Shaw; Edward J Lammer
Journal:  Am J Med Genet A       Date:  2013-10-11       Impact factor: 2.802

2.  ZFHX4 interacts with the NuRD core member CHD4 and regulates the glioblastoma tumor-initiating cell state.

Authors:  Yakov Chudnovsky; Dohoon Kim; Siyuan Zheng; Warren A Whyte; Mukesh Bansal; Mark-Anthony Bray; Shuba Gopal; Matthew A Theisen; Steve Bilodeau; Prathapan Thiru; Julien Muffat; Omer H Yilmaz; Maya Mitalipova; Kevin Woolard; Jeongwu Lee; Riko Nishimura; Nobuo Sakata; Howard A Fine; Anne E Carpenter; Serena J Silver; Roel G W Verhaak; Andrea Califano; Richard A Young; Keith L Ligon; Ingo K Mellinghoff; David E Root; David M Sabatini; William C Hahn; Milan G Chheda
Journal:  Cell Rep       Date:  2014-01-16       Impact factor: 9.423

3.  Characterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotype.

Authors:  María Palomares; Alicia Delicado; Elena Mansilla; María Luisa de Torres; Elena Vallespín; Luis Fernandez; Victor Martinez-Glez; Sixto García-Miñaur; Julián Nevado; Fernando Santos Simarro; Victor L Ruiz-Perez; Sally Ann Lynch; Freddie H Sharkey; Ann-Charlotte Thuresson; Göran Annerén; Elga F Belligni; María Luisa Martínez-Fernández; Eva Bermejo; Beata Nowakowska; Anna Kutkowska-Kazmierczak; Ewa Bocian; Ewa Obersztyn; María Luisa Martínez-Frías; Raoul C M Hennekam; Pablo Lapunzina
Journal:  Am J Hum Genet       Date:  2011-07-28       Impact factor: 11.025

4.  Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family.

Authors:  Mitsuko Nakashima; Motoi Nakano; Akiyoshi Hirano; Tatsuya Kishino; Shinji Kondoh; Nobutomo Miwa; Norio Niikawa; Koh-Ichiro Yoshiura
Journal:  J Hum Genet       Date:  2007-11-07       Impact factor: 3.172

5.  A survey of well conserved families of C2H2 zinc-finger genes in Daphnia.

Authors:  Arun Seetharam; Yang Bai; Gary W Stuart
Journal:  BMC Genomics       Date:  2010-04-30       Impact factor: 3.969

6.  Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics.

Authors:  Mauro Longoni; Frances A High; Meaghan K Russell; Alireza Kashani; Adam A Tracy; Caroline M Coletti; Regis Hila; Ahmed Shamia; Julie Wells; Kate G Ackerman; Jay M Wilson; Carol J Bult; Charles Lee; Kasper Lage; Barbara R Pober; Patricia K Donahoe
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-08       Impact factor: 11.205

7.  Identification of Drosophila Zfh2 as a Mediator of Hypercapnic Immune Regulation by a Genome-Wide RNA Interference Screen.

Authors:  Iiro Taneli Helenius; Ryan J Haake; Yong-Jae Kwon; Jennifer A Hu; Thomas Krupinski; S Marina Casalino-Matsuda; Peter H S Sporn; Jacob I Sznajder; Greg J Beitel
Journal:  J Immunol       Date:  2015-12-07       Impact factor: 5.422

Review 8.  8q21.11 microdeletion in two patients with syndromic peters anomaly.

Authors:  Hannah Happ; Kala F Schilter; Eric Weh; Linda M Reis; Elena V Semina
Journal:  Am J Med Genet A       Date:  2016-07-05       Impact factor: 2.802

9.  Key genes for modulating information flow play a temporal role as breast tumor coexpression networks are dynamically rewired by letrozole.

Authors:  Nadia M Penrod; Jason H Moore
Journal:  BMC Med Genomics       Date:  2013-05-07       Impact factor: 3.063

10.  Ablation of Zfhx4 results in early postnatal lethality by disrupting the respiratory center in mice.

Authors:  Meiqin Zhang; Sichen Du; Huayuan Ou; Renjie Cui; Nan Jiang; Yifeng Lin; Runsheng Ge; Duan Ma; Jin Zhang
Journal:  J Mol Cell Biol       Date:  2021-07-06       Impact factor: 6.216

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