Literature DB >> 10598820

Identification, mapping, and genomic structure of a novel X-chromosomal human gene (SMPX) encoding a small muscular protein.

D Patzak1, O Zhuchenko, C C Lee, M Wehnert.   

Abstract

Reciprocal probing has been used to identify a cDNA clone (xh8H11) representing a gene preferentially expressed in striated muscle. The gene maps close to DXS7101 31.9 cM from the short arm telomere of the X-chromosome at Xp22.1. On searching expressed and genomic databases, 21 expressed sequence tags were found that allowed the assignment of a human extended consensus sequence of 887 bp, suggesting a completely expressed gene symbolized as SMPX. By using the human consensus sequence, the orthologous mouse Smpx and rat SMPX genes could be aligned and confirmed by complete sequencing of additional SMPX-related clones obtained by library screening. An open reading frame was identified encoding a peptide of 88-86 and 85 amino acids in human and rodents, respectively. The predicted peptide had no significant homologies to known structural elements. The human consensus cDNA sequence was used to define the genomic structure of the human SMPX that had been missed by a previous large scale sequencing approach. The gene consists of five exons (> or =172, 57, 84, 148, > or =422 bp) and four introns (3639, 10410, 6052, 31134 bp) comprising together 52.1 kb and is preferentially and abundantly expressed in heart and skeletal muscle. Thus, a novel human gene encoding a small muscular protein that maps to Xp22.1 (SMPX) has been identified and structurally characterized as a basis for further functional analysis.

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Year:  1999        PMID: 10598820     DOI: 10.1007/s004390051138

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  13 in total

Review 1.  Are histochemistry and cytochemistry 'Omics'?

Authors:  Gary Coulton
Journal:  J Mol Histol       Date:  2004-08       Impact factor: 2.611

2.  A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family.

Authors:  Yuyuan Deng; Zhijie Niu; LiangLiang Fan; Jie Ling; Hongsheng Chen; Xinzhang Cai; Lingyun Mei; Chufeng He; Xuewei Zhang; Jie Wen; Meng Li; Wu Li; Taoxi Li; Shushan Sang; Yalan Liu; Yong Feng
Journal:  J Hum Genet       Date:  2018-03-20       Impact factor: 3.172

3.  Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss.

Authors:  Antje K Huebner; Marta Gandia; Peter Frommolt; Anika Maak; Eva M Wicklein; Holger Thiele; Janine Altmüller; Florian Wagner; Antonio Viñuela; Luis A Aguirre; Felipe Moreno; Hannes Maier; Isabella Rau; Sebastian Giesselmann; Gudrun Nürnberg; Andreas Gal; Peter Nürnberg; Christian A Hübner; Ignacio del Castillo; Ingo Kurth
Journal:  Am J Hum Genet       Date:  2011-05-05       Impact factor: 11.025

4.  Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment.

Authors:  Margit Schraders; Stefan A Haas; Nicole J D Weegerink; Jaap Oostrik; Hao Hu; Lies H Hoefsloot; Sriram Kannan; Patrick L M Huygen; Ronald J E Pennings; Ronald J C Admiraal; Vera M Kalscheuer; Henricus P M Kunst; Hannie Kremer
Journal:  Am J Hum Genet       Date:  2011-05-05       Impact factor: 11.025

Review 5.  Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.

Authors:  Rahul Mittal; Amit P Patel; Desiree Nguyen; Debbie R Pan; Vasanti M Jhaveri; Jason R Rudman; Arjuna Dharmaraja; Denise Yan; Yong Feng; Prem Chapagain; David J Lee; Susan H Blanton; Xue Zhong Liu
Journal:  Gene       Date:  2018-01-10       Impact factor: 3.688

6.  The small muscle-specific protein Csl modifies cell shape and promotes myocyte fusion in an insulin-like growth factor 1-dependent manner.

Authors:  S Palmer; N Groves; A Schindeler; T Yeoh; C Biben; C C Wang; D B Sparrow; L Barnett; N A Jenkins; N G Copeland; F Koentgen; T Mohun; R P Harvey
Journal:  J Cell Biol       Date:  2001-05-28       Impact factor: 10.539

Review 7.  Genetics of Nonsyndromic Congenital Hearing Loss.

Authors:  Oguz Kadir Egilmez; M Tayyar Kalcioglu
Journal:  Scientifica (Cairo)       Date:  2016-02-18

8.  A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.

Authors:  Zhijie Niu; Yong Feng; Lingyun Mei; Jie Sun; Xueping Wang; Juncheng Wang; Zhengmao Hu; Yunpeng Dong; Hongsheng Chen; Chufeng He; Yalan Liu; Xinzhang Cai; Xuezhong Liu; Lu Jiang
Journal:  PLoS One       Date:  2017-05-25       Impact factor: 3.240

9.  Overexpression of SMPX in adult skeletal muscle does not change skeletal muscle fiber type or size.

Authors:  Einar Eftestøl; Tine Norman Alver; Kristian Gundersen; Jo C Bruusgaard
Journal:  PLoS One       Date:  2014-06-17       Impact factor: 3.240

10.  The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation.

Authors:  Beatriz Ferrán; Ingrid Martí-Pàmies; Judith Alonso; Ricardo Rodríguez-Calvo; Silvia Aguiló; Francisco Vidal; Cristina Rodríguez; José Martínez-González
Journal:  Sci Rep       Date:  2016-05-16       Impact factor: 4.379

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