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MACF1 gene structure: a hybrid of plectin and dystrophin

dc.contributor.authorGong, Tzy-Wen L.en_US
dc.contributor.authorBesirli, Cagri G.en_US
dc.contributor.authorLomax, Margaret I.en_US
dc.date.accessioned2006-09-08T19:59:41Z
dc.date.available2006-09-08T19:59:41Z
dc.date.issued2001-11en_US
dc.identifier.citationGong, Tzy-Wen L.; Besirli, Cagri G.; Lomax, Margaret I.; (2001). "MACF1 gene structure: a hybrid of plectin and dystrophin." Mammalian Genome 12(11): 852-861. <http://hdl.handle.net/2027.42/42123>en_US
dc.identifier.issn0938-8990en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42123
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11845288&dopt=citationen_US
dc.description.abstractMammalian MACF1 (Macrophin1; previously named ACF7) is a giant cytoskeletal linker protein with three known isoforms that arise by alternative splicing. We isolated a 19.1-kb cDNA encoding a fourth isoform (MACF1-4) with a unique N-terminus. Instead of an N-terminal actin-binding domain found in the other three isoforms, MACF1-4 has eight plectin repeats. The MACF1 gene is located on human Chr 1p32, contains at least 102 exons, spans over 270 kb, and gives rise to four major isoforms with different N-termini. The genomic organization of the actin-binding domain is highly conserved in mammalian genes for both plectin and BPAG1. All eight plectin repeats are encoded by one large exon; this feature is similar to the genomic structure of plectin. The intron positions within spectrin repeats in MACF1 are very similar to those in the dystrophin gene. This demonstrates that MACF1 has characteristic features of genes for two classes of cytoskeletal proteins, i.e., plectin and dystrophin.en_US
dc.format.extent1085780 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag New York Inc.en_US
dc.subject.otherLegacyen_US
dc.titleMACF1 gene structure: a hybrid of plectin and dystrophinen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumKresge Hearing Research Institute, Department of Otolaryngology/Head Neck Surgery, 9301E MSRB III, 1150 W. Medical Center Dr., Box 0648, University of Michigan, Ann Arbor, MI 48109-0648, USA, USen_US
dc.contributor.affiliationumKresge Hearing Research Institute, Department of Otolaryngology/Head Neck Surgery, 9301E MSRB III, 1150 W. Medical Center Dr., Box 0648, University of Michigan, Ann Arbor, MI 48109-0648, USA, USen_US
dc.contributor.affiliationumKresge Hearing Research Institute, Department of Otolaryngology/Head Neck Surgery, 9301E MSRB III, 1150 W. Medical Center Dr., Box 0648, University of Michigan, Ann Arbor, MI 48109-0648, USA, USen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid11845288en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42123/1/335-12-11-852_10120852.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00335-001-3037-3en_US
dc.identifier.sourceMammalian Genomeen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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