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          Institute: MPI für molekulare Genetik     Collection: Department of Vertebrate Genomics     Display Documents



  history
ID: 271588.0, MPI für molekulare Genetik / Department of Vertebrate Genomics
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients
Authors:Horváth, Judit; Fliegauf, Manfred; Olbrich, Heike; Kispert, Andreas; King, Stephen M.; Mitchison, Hannah; Zariwala, Maimoona A.; Knowles, Michael R.; Sudbrak, Ralf; Fekete, György; Neesen, Juergen; Reinhardt, Richard; Omran, Heymut
Language:English
Date of Publication (YYYY-MM-DD):2005-04-21
Title of Journal:American Journal of Respiratory Cell and Molecular Biology
Journal Abbrev.:Am J Respir Cell Mol Biol
Volume:33
Issue / Number:1
Start Page:41
End Page:47
Copyright:© 2005 American Thoracic Society
Review Status:not specified
Audience:Experts Only
Abstract / Description:Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder characterized by chronic infections of the upper and lower airways, randomization of left/right body asymmetry, and reduced fertility. The phenotype results from dysfunction of motile cilia of the respiratory epithelium, at the embryonic node and of sperm flagella. Ultrastructural defects often involve outer dynein arms (ODAs), that are composed of several light (LCs), intermediate, and heavy (HCs) dynein chains. We recently showed that recessive mutations of DNAH5, the human ortholog of the biflagellate Chlamydomonas ODA {gamma}-HC, cause PCD. In Chlamydomonas, motor protein activity of the {gamma}-ODA-HC is regulated by binding of the axonemal LC1. We report the identification of the human (DNAL1) and murine (Dnal1) orthologs of the Chlamydomonas LC1-gene. Northern blot and in situ hybridization analyses revealed specific expression in testis, embryonic node, respiratory epithelium, and ependyma, resembling the DNAH5 expression pattern. In silico protein analysis showed complete conservation of the LC1/{gamma}-HC binding motif in DNAL1. Protein interaction studies demonstrated binding of DNAL1 and DNAH5. Based on these findings, we considered DNAL1 a candidate for PCD and sequenced all exons of DNAL1 in 86 patients. Mutational analysis was negative, excluding a major role of DNAL1 in the pathogenesis of PCD.
Free Keywords:cilia; primary ciliary dyskinesia; light chain; dynein
Comment of the Author/Creator:Email: omran@kikli.ukl.uni-freiburg.de
External Publication Status:published
Document Type:Article
Communicated by:Hans Lehrach
Affiliations:MPI für molekulare Genetik
External Affiliations:Department of Pediatrics and Adolescent Medicine, Albert-Ludwigs-University, Freiburg;
Institut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover;
Institute of Human Genetics, University of Goettingen, Goettingen, Germany;
Department of Biochemistry, University of Connecticut Health Center, Farmington, Connecticut;
Department of Medicine, University of North Carolina, Chapel Hill, North Carolina;
Department of Paediatrics and Child Health, Royal Free and University College Medical School London, London, United Kingdom;
Second Department of Pediatrics, School of Medicine, Semmelweis University, Budapest, Hungary
Identifiers:ISSN:1044-1549
DOI:10.1165/rcmb.2004-0335OC
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