Literature DB >> 23449628

Overdosage of Hand2 causes limb and heart defects in the human chromosomal disorder partial trisomy distal 4q.

Masaru Tamura1, Masaki Hosoya, Motoi Fujita, Tomoko Iida, Takanori Amano, Akiteru Maeno, Taro Kataoka, Taketo Otsuka, Shigekazu Tanaka, Shuichi Tomizawa, Toshihiko Shiroishi.   

Abstract

Partial trisomy distal 4q (denoted 4q+) is a human chromosomal disorder caused by duplication of the distal end of the long arm of chromosome 4 (Chr4). This disorder manifests typical phenotypes, including craniofacial, renal, heart and thumb developmental defects. Although these clinical features are likely caused by a dosage imbalance in the gene network involving the trisomic region, the causative gene or genes and the molecular bases are largely unknown. Here, we report mouse Recombination-induced mutation 4 (Rim4) as a model animal of 4q+. The Rim4 genome contains an insertion of a 6.5 Mb fragment from mouse chromosome 8 into chromosome 6. This insertion fragment contains 17 genes, including Hand2, that encode the basic helix-loop-helix transcription factor and is syntenic to the distal end of human Chr4, 4q32.3 to 4q34.1, which is responsible for 4q+. A comparison of phenotypes between patients with Rim4 and 4q+ revealed that Rim4 shows direct parallels with many phenotypes of 4q+ such as craniofacial, heart, cervical vertebra and limb deformities. Rebalancing the gene dosage by a genetic cross with Hand2 knockout mice ameliorated symptoms of the heart and limb deformities of Rim4. Conversely, an increase in copy number of Hand2 in wild-type mice recaptures the heart and limb deformities of Rim4. Our results collectively demonstrate that overdosage of Hand2 is a major cause for at least the limb and heart phenotypes of 4q+ and that mouse Rim4 provides a unique animal model for understanding the molecular bases underlying the complex phenotypes of 4q+.

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Year:  2013        PMID: 23449628     DOI: 10.1093/hmg/ddt099

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  20 in total

1.  Gene network and familial analyses uncover a gene network involving Tbx5/Osr1/Pcsk6 interaction in the second heart field for atrial septation.

Authors:  Ke K Zhang; Menglan Xiang; Lun Zhou; Jielin Liu; Nathan Curry; Damian Heine Suñer; Pablo Garcia-Pavia; Xiaohua Zhang; Qin Wang; Linglin Xie
Journal:  Hum Mol Genet       Date:  2016-01-06       Impact factor: 6.150

Review 2.  The two domain hypothesis of limb prepattern and its relevance to congenital limb anomalies.

Authors:  Hirotaka Tao; Yasuhiko Kawakami; Chi-Chung Hui; Sevan Hopyan
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2017-03-20       Impact factor: 5.814

3.  Hand Factors in Cardiac Development.

Authors:  Rajani M George; Anthony B Firulli
Journal:  Anat Rec (Hoboken)       Date:  2018-10-05       Impact factor: 2.064

4.  Hand2 elevates cardiomyocyte production during zebrafish heart development and regeneration.

Authors:  Yocheved L Schindler; Kristina M Garske; Jinhu Wang; Beth A Firulli; Anthony B Firulli; Kenneth D Poss; Deborah Yelon
Journal:  Development       Date:  2014-07-18       Impact factor: 6.868

5.  Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.

Authors:  Tingting Song; Shanning Wan; Yu Li; Ying Xu; Yinghui Dang; Yunyun Zheng; Chunyan Li; Jiao Zheng; Biliang Chen; Jianfang Zhang
Journal:  J Clin Lab Anal       Date:  2018-07-25       Impact factor: 2.352

6.  Automatic classification framework for ventricular septal defects: a pilot study on high-throughput mouse embryo cardiac phenotyping.

Authors:  Zhongliu Xie; Xi Liang; Liucheng Guo; Asanobu Kitamoto; Masaru Tamura; Toshihiko Shiroishi; Duncan Gillies
Journal:  J Med Imaging (Bellingham)       Date:  2015-09-11

7.  HAND transcription factors cooperatively specify the aorta and pulmonary trunk.

Authors:  Joshua W Vincentz; Beth A Firulli; Kevin P Toolan; Marco Osterwalder; Len A Pennacchio; Anthony B Firulli
Journal:  Dev Biol       Date:  2021-03-20       Impact factor: 3.148

8.  The Transcription Factor Hand1 Is Involved In Runx2-Ihh-Regulated Endochondral Ossification.

Authors:  Lindsay E Laurie; Hiroki Kokubo; Masataka Nakamura; Yumiko Saga; Noriko Funato
Journal:  PLoS One       Date:  2016-02-26       Impact factor: 3.240

9.  Functionally significant, rare transcription factor variants in tetralogy of Fallot.

Authors:  Ana Töpf; Helen R Griffin; Elise Glen; Rachel Soemedi; Danielle L Brown; Darroch Hall; Thahira J Rahman; Jyrki J Eloranta; Christoph Jüngst; A Graham Stuart; John O'Sullivan; Bernard D Keavney; Judith A Goodship
Journal:  PLoS One       Date:  2014-08-05       Impact factor: 3.240

Review 10.  Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Authors:  Barbara Vona; Indrajit Nanda; Cordula Neuner; Jörg Schröder; Vera M Kalscheuer; Wafaa Shehata-Dieler; Thomas Haaf
Journal:  BMC Med Genet       Date:  2014-06-25       Impact factor: 2.103

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