Literature DB >> 7665173

Assignment of cardiac homeobox gene CSX to human chromosome 5q34.

I Shiojima1, I Komuro, J Inazawa, Y Nakahori, I Matsushita, T Abe, R Nagai, Y Yazaki.   

Abstract

Homeobox-containing genes play critical roles in regulating tissue-specific gene expression essential for tissue differentiation, as well as determining the temporal and spatial patterns of development. Recently, a human cardiac homeobox-containing gene, CSX, has been isolated. CSX is abundantly expressed in the human heart from fetal stages, suggesting that CSX plays an important role in human heart formation. In the present study, we have determined the chromosomal localization of CSX by fluorescence in situ hybridization techniques and systemic screening of a yeast artificial chromosome library using polymerase chain reaction. By these methods, CSX was mapped to 5q34 of human chromosome 5 near the boundary of 5q34 and 5q35. In this region, another homeobox-containing gene MSX2, which is expressed in various tissues including the conduction system of the developing heart, has been assigned. Localization of CSX and MSX2 to the same region of the human chromosome suggests that these genes may be coordinately regulated during human heart formation.

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Year:  1995        PMID: 7665173     DOI: 10.1006/geno.1995.1027

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


  11 in total

1.  Integration of four genes, a pseudogene, thirty-one STSs, and a highly polymorphic STRP into the 7-10 Mb YAC contig of 5q34-q35.

Authors:  M Kostrzewa; D L Grady; R K Moyzis; L Flöter; U Müller
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

2.  Notch signalling in cardiovasculogenesis: insight into their role in early cardiovascular development.

Authors:  Marimuthu Saravanakumar; Halagowder Devaraj
Journal:  Mol Biol Rep       Date:  2012-12-27       Impact factor: 2.316

Review 3.  Electrical disorders in atrial septal defect: genetics and heritability.

Authors:  Hisaaki Aoki; Minoru Horie
Journal:  J Thorac Dis       Date:  2018-09       Impact factor: 2.895

4.  Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.

Authors:  Hong Yu; Jia-Hong Xu; Hao-Ming Song; Lan Zhao; Wen-Jun Xu; Juan Wang; Ruo-Gu Li; Lei Xu; Wei-Feng Jiang; Xing-Biao Qiu; Jin-Qi Jiang; Xin-Kai Qu; Xu Liu; Wei-Yi Fang; Jin-Fa Jiang; Yi-Qing Yang
Journal:  Int J Med Sci       Date:  2014-04-07       Impact factor: 3.738

5.  Genome-wide analysis reveals conserved transcriptional responses downstream of resting potential change in Xenopus embryos, axolotl regeneration, and human mesenchymal cell differentiation.

Authors:  Vaibhav P Pai; Christopher J Martyniuk; Karen Echeverri; Sarah Sundelacruz; David L Kaplan; Michael Levin
Journal:  Regeneration (Oxf)       Date:  2015-11-26

6.  Computational modeling suggests impaired interactions between NKX2.5 and GATA4 in individuals carrying a novel pathogenic D16N NKX2.5 mutation.

Authors:  Saidulu Mattapally; Mrityunjay Singh; Kona Samba Murthy; Shailendra Asthana; Sanjay K Banerjee
Journal:  Oncotarget       Date:  2018-02-09

7.  Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3.

Authors:  Aleksander Jamsheer; Anna Sowińska; Dorota Simon; Małgorzata Jamsheer-Bratkowska; Tomasz Trzeciak; Anna Latos-Bieleńska
Journal:  BMC Med Genet       Date:  2013-01-24       Impact factor: 2.103

8.  Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.

Authors:  Wen-Hui Xie; Cheng Chang; Ying-Jia Xu; Ruo-Gu Li; Xin-Kai Qu; Wei-Yi Fang; Xu Liu; Yi-Qing Yang
Journal:  Clinics (Sao Paulo)       Date:  2013-06       Impact factor: 2.365

9.  A case report of truncus arteriosus communis and genetic counseling.

Authors:  Gholamreza Nourzad; Mahnaz Baghershiroodi
Journal:  ARYA Atheroscler       Date:  2013-06

10.  Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease.

Authors:  Mehri Khatami; Mansoureh Mazidi; Shabnam Taher; Mohammad Mehdi Heidari; Mehdi Hadadzadeh
Journal:  Medicina (Kaunas)       Date:  2018-06-19       Impact factor: 2.430

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