Abstract
A new member of the dystrobrevin gene family was identified using a bioinformatics approach. Sequence analysis indicates that this gene, named DTN-B, is highly homologous to the rabbit A0, the previously described dystrobrevin (DTN), Torpedo 87 kDa and to the C-terminus of dystrophin. The coiled-coil domain, shown to be the site of interaction between dystrobrevins and dystrophin, is highly conserved. Immunostaining studies indicate that DTN-B and DTN expression is absent in affected muscle fibers from DMD patients and carriers.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Amino Acid Sequence
-
Animals
-
Blotting, Northern
-
Blotting, Western
-
Chromosome Mapping
-
Chromosomes, Artificial, Yeast
-
Chromosomes, Human, Pair 2
-
DNA, Complementary
-
Dystrophin-Associated Proteins*
-
Heterozygote
-
Humans
-
In Situ Hybridization, Fluorescence
-
Mice
-
Molecular Sequence Data
-
Multigene Family*
-
Muscle, Skeletal / metabolism
-
Muscular Dystrophies / genetics
-
Neuropeptides / genetics*
-
RNA Splicing
-
Rabbits
-
Sequence Homology, Amino Acid
-
Tumor Cells, Cultured
Substances
-
DNA, Complementary
-
DTNB protein, human
-
Dystrophin-Associated Proteins
-
Neuropeptides
Associated data
-
GENBANK/Y12712
-
GENBANK/Y15718
-
GENBANK/Y15719
-
GENBANK/Y15720
-
GENBANK/Y15721
-
GENBANK/Y15722
-
GENBANK/Y15742