Literature DB >> 11175280

Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes.

A K Maiti1, M G Mattéi, M Jorissen, A Volz, A Zeigler, P Bouvagnet.   

Abstract

Sliding between adjacent microtubules within the axonema gives rise to the motility of cilia and flagella. The driving force is produced by dynein complexes which are mainly composed of the axonemal dynein heavy chains. We used cells of human respiratory epithelium after in vitro ciliogenesis to clone cDNA fragments of nine dynein heavy chain genes, one of which had never been identified before. Dynein heavy chains are highly conserved from protozoa to human and the evolutionary ancestry of these dynein heavy chain cDNA fragments was deduced by phylogenetic analysis. These dynein heavy chain cDNAs are highly transcribed in human tissues containing axonema such as trachea, testis and brain, but not in adult heart or placenta. PAC clones containing dynein heavy chains were obtained and used to determine by FISH their chromosomal position in the human genome. They were mapped to 2p12-p11, 2q33, 3p21.2-p21.1, 13q14, 16p12 and 17p12. The chromosomal assignment of these dynein heavy chain genes which was confirmed by GeneBridge 4 radiation hybrid screening, will be extremely useful for linkage analysis efforts in patients with primary ciliary dyskinesia (PCD).

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Year:  2000        PMID: 11175280     DOI: 10.1038/sj.ejhg.5200555

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  22 in total

1.  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

2.  The axonemal dynein heavy chain 10 gene is essential for monocilia motility and spine alignment in zebrafish.

Authors:  Yunjia Wang; Benjamin R Troutwine; Hongqi Zhang; Ryan S Gray
Journal:  Dev Biol       Date:  2021-12-13       Impact factor: 3.582

3.  Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility.

Authors:  Kuokuo Li; Guanxiong Wang; Mingrong Lv; Jieyu Wang; Yang Gao; Fei Tang; Chuan Xu; Wen Yang; Hui Yu; Zhongmei Shao; Hao Geng; Qing Tan; Qunshan Shen; Dongdong Tang; Xiaoqing Ni; Tianjuan Wang; Bing Song; Huan Wu; Ran Huo; Zhiguo Zhang; Yuping Xu; Ping Zhou; Fangbiao Tao; Zhaolian Wei; Xiaojin He; Yunxia Cao
Journal:  J Assist Reprod Genet       Date:  2021-10-16       Impact factor: 3.412

4.  Phosphorylation-dependent proteome of Marcks in ependyma during aging and behavioral homeostasis in the mouse forebrain.

Authors:  Nagendran Muthusamy; Taufika I Williams; Ryan O'Toole; Jon J Brudvig; Kenneth B Adler; Jill M Weimer; David C Muddiman; H Troy Ghashghaei
Journal:  Geroscience       Date:  2022-01-24       Impact factor: 7.581

5.  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

6.  Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.

Authors:  Mariem Ben Khelifa; Charles Coutton; Raoudha Zouari; Thomas Karaouzène; John Rendu; Marie Bidart; Sandra Yassine; Virginie Pierre; Julie Delaroche; Sylviane Hennebicq; Didier Grunwald; Denise Escalier; Karine Pernet-Gallay; Pierre-Simon Jouk; Nicolas Thierry-Mieg; Aminata Touré; Christophe Arnoult; Pierre F Ray
Journal:  Am J Hum Genet       Date:  2013-12-19       Impact factor: 11.025

Review 7.  Primary ciliary dyskinesia: recent advances in pathogenesis, diagnosis and treatment.

Authors:  Hauw Lie; Thomas Ferkol
Journal:  Drugs       Date:  2007       Impact factor: 9.546

8.  Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans.

Authors:  Roshni R Singaraja; Ian Tietjen; G Kees Hovingh; Patrick L Franchini; Chris Radomski; Kenny Wong; Margaret vanHeek; Ioannis M Stylianou; Linus Lin; Liangsu Wang; Lyndon Mitnaul; Brian Hubbard; Michael Winther; Maryanne Mattice; Annick Legendre; Robin Sherrington; John J Kastelein; Karen Akinsanya; Andrew Plump; Michael R Hayden
Journal:  J Lipid Res       Date:  2014-06-02       Impact factor: 5.922

9.  Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing.

Authors:  Jonathan S Berg; James P Evans; Margaret W Leigh; Heymut Omran; Chris Bizon; Ketan Mane; Michael R Knowles; Karen E Weck; Maimoona A Zariwala
Journal:  Genet Med       Date:  2011-03       Impact factor: 8.822

10.  Isolation, in silico characterization and chromosomal localization of a group of cDNAs from ciliated epithelial cells after in vitro ciliogenesis.

Authors:  A K Maiti; M Jorissen; P Bouvagnet
Journal:  Genome Biol       Date:  2001-06-27       Impact factor: 13.583

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