Literature DB >> 10405324

A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24.

P Ianakiev1, M W Kilpatrick, C Dealy, R Kosher, J R Korenberg, X N Chen, P Tsipouras.   

Abstract

We report the cloning and characterization of a new human gene, Dactylin, encoding a novel member of the F-box/WD40 protein family. The Dactylin gene comprises nine exons distributed in more than 85 kb of genomic DNA and encoding a protein with four WD40 repeats and an F-box motif. Northern blot analysis demonstrates a single 2.8 kb transcript in brain, kidney, lung and liver. FISH hybridization localized Dactylin to 10q24.3. Using an Msc I SNP identified in the first exon of the gene, we were able to assign Dactylin within the critical region for Split Hand Split Foot malformation (SHFM3) that has been mapped to 10q24. The SHFM3 phenotype includes absence or hypoplasia of the central digital rays, a deep median cleft and syndactyly of the remaining digits. Recent studies have demonstrated the importance of F-box/WD40 proteins in the regulation of developmental processes, by a mechanism of specific ubiquitinization and subsequent proteolysis of target proteins belonging to the Wnt, Hh and NF-kappaB signaling pathways. The chromosomal location of Dactylin and its putative function as an F-box/WD40 repeat protein, likely to be involved in key signaling pathways crucial for normal limb development, make it a promising candidate gene for SHFM3. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10405324     DOI: 10.1006/bbrc.1999.0963

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  9 in total

1.  Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

Authors:  P Ianakiev; M W Kilpatrick; I Toudjarska; D Basel; P Beighton; P Tsipouras
Journal:  Am J Hum Genet       Date:  2000-06-05       Impact factor: 11.025

Review 2.  Ubiquitination-mediated degradation of cell cycle-related proteins by F-box proteins.

Authors:  Nana Zheng; Zhiwei Wang; Wenyi Wei
Journal:  Int J Biochem Cell Biol       Date:  2016-02-06       Impact factor: 5.085

3.  Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.

Authors:  Hiroki Kano; Kenji Kurosawa; Emiko Horii; Shiro Ikegawa; Hideki Yoshikawa; Hiroki Kurahashi; Tatsushi Toda
Journal:  Hum Genet       Date:  2005-10-19       Impact factor: 4.132

4.  Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype.

Authors:  Hiroki Kano; Hiroki Kurahashi; Tatsushi Toda
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-05       Impact factor: 11.205

5.  A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.

Authors:  Christian Babbs; Raoul Heller; David B Everman; Mark Crocker; Stephen R F Twigg; Charles E Schwartz; Henk Giele; Andrew O M Wilkie
Journal:  Hum Genet       Date:  2007-06-14       Impact factor: 4.132

6.  The novel ubiquitin ligase complex, SCF(Fbxw4), interacts with the COP9 signalosome in an F-box dependent manner, is mutated, lost and under-expressed in human cancers.

Authors:  William W Lockwood; Sahiba K Chandel; Greg L Stewart; Hediye Erdjument-Bromage; Levi J Beverly
Journal:  PLoS One       Date:  2013-05-02       Impact factor: 3.240

7.  Circular RNA circFBXW4 suppresses hepatic fibrosis via targeting the miR-18b-3p/FBXW7 axis.

Authors:  Xin Chen; Hai-Di Li; Fang-Tian Bu; Xiao-Feng Li; Yu Chen; Sai Zhu; Jia-Nan Wang; Si-Yu Chen; Ying-Yin Sun; Xue-Yin Pan; Na-Na Yin; Jie-Jie Xu; Cheng Huang; Jun Li
Journal:  Theranostics       Date:  2020-03-26       Impact factor: 11.556

8.  Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation.

Authors:  Li Dai; Ying Deng; Nana Li; Liang Xie; Meng Mao; Jun Zhu
Journal:  BMC Med Genet       Date:  2013-04-18       Impact factor: 2.103

9.  FBXW4 Acts as a Protector of FOLFOX-Based Chemotherapy in Metastatic Colorectal Cancer Identified by Co-Expression Network Analysis.

Authors:  Yiyi Zhang; Lijun Sun; Xiaojie Wang; Yanwu Sun; Ying Chen; Meifang Xu; Pan Chi; Xingrong Lu; Zongbin Xu
Journal:  Front Genet       Date:  2020-03-11       Impact factor: 4.599

  9 in total

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