Literature DB >> 9256245

Isolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment.

C Chapelin1, B Duriez, F Magnino, M Goossens, E Escudier, S Amselem.   

Abstract

Dynein heavy chains (DHCs) are the main components of multisubunit motor ATPase complexes called dyneins. Axonemal dyneins provide the driving force for ciliary and flagellar motility. Recent molecular studies demonstrated that multiple DHC isoforms are produced by separate genes. We describe the isolation of five human axonemal DHC genes. Analysis of the human genomic clones revealed the existence of intronic sequences that were used to demonstrate that human axonemal DHC genes are located on different chromosomes. The cloned human DHC sequences were integrated into an evolutionary approach based on phylogenetic analysis. Tissue expression studies showed that these human axonemal DHCs are expressed in testis and/or trachea, two tissues with axonemal structures that can be altered in primary ciliary dyskinesia, making DHC genes strong candidates in the genesis of these human diseases.

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Year:  1997        PMID: 9256245     DOI: 10.1016/s0014-5793(97)00800-4

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  18 in total

1.  A locus for primary ciliary dyskinesia maps to chromosome 19q.

Authors:  M Meeks; A Walne; S Spiden; H Simpson; H Mussaffi-Georgy; H D Hamam; E L Fehaid; M Cheehab; M Al-Dabbagh; S Polak-Charcon; H Blau; A O'Rawe; H M Mitchison; R M Gardiner; E Chung
Journal:  J Med Genet       Date:  2000-04       Impact factor: 6.318

2.  Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome).

Authors:  C Guichard; M C Harricane; J J Lafitte; P Godard; M Zaegel; V Tack; G Lalau; P Bouvagnet
Journal:  Am J Hum Genet       Date:  2001-02-23       Impact factor: 11.025

3.  Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

Authors:  G Pennarun; E Escudier; C Chapelin; A M Bridoux; V Cacheux; G Roger; A Clément; M Goossens; S Amselem; B Duriez
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

4.  Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia.

Authors:  Manfred Fliegauf; Heike Olbrich; Judit Horvath; Johannes H Wildhaber; Maimoona A Zariwala; Marcus Kennedy; Michael R Knowles; Heymut Omran
Journal:  Am J Respir Crit Care Med       Date:  2005-03-04       Impact factor: 21.405

5.  Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.

Authors:  Ozanna Burnicka-Turek; Jeffrey D Steimle; Wenhui Huang; Lindsay Felker; Anna Kamp; Junghun Kweon; Michael Peterson; Roger H Reeves; Cheryl L Maslen; Peter J Gruber; Xinan H Yang; Jay Shendure; Ivan P Moskowitz
Journal:  Hum Mol Genet       Date:  2016-06-23       Impact factor: 6.150

6.  Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease.

Authors:  Dandi Qiao; Christoph Lange; Terri H Beaty; James D Crapo; Kathleen C Barnes; Michael Bamshad; Craig P Hersh; Jarrett Morrow; Victor M Pinto-Plata; Nathaniel Marchetti; Raphael Bueno; Bartolome R Celli; Gerald J Criner; Edwin K Silverman; Michael H Cho
Journal:  Am J Respir Crit Care Med       Date:  2016-06-15       Impact factor: 21.405

7.  Variation in DNAH1 may contribute to primary ciliary dyskinesia.

Authors:  Faiqa Imtiaz; Rabab Allam; Khushnooda Ramzan; Moeenaldeen Al-Sayed
Journal:  BMC Med Genet       Date:  2015-03-17       Impact factor: 2.103

8.  Whole exome sequencing in females with autism implicates novel and candidate genes.

Authors:  Merlin G Butler; Syed K Rafi; Waheeda Hossain; Dietrich A Stephan; Ann M Manzardo
Journal:  Int J Mol Sci       Date:  2015-01-07       Impact factor: 5.923

9.  Altered gene expression in glycolysis-cholesterol synthesis axis correlates with outcome of triple-negative breast cancer.

Authors:  Peng-Cheng Zhong; Rong Shu; Hui-Wen Wu; Zhi-Wen Liu; Xiao-Ling Shen; Ying-Jie Hu
Journal:  Exp Biol Med (Maywood)       Date:  2020-11-27

10.  A novel splicing variant in DNAH8 causes asthenozoospermia.

Authors:  Zhou Zhou; Xiaoyan Mao; Biaobang Chen; Jian Mu; Wenjing Wang; Bin Li; Zheng Yan; Jie Dong; Qiaoli Li; Yanping Kuang; Lei Wang; Ling Wu; Qing Sang
Journal:  J Assist Reprod Genet       Date:  2021-02-20       Impact factor: 3.357

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