Literature DB >> 10893187

Assembly of multiple dystrobrevin-containing complexes in the kidney.

N Y Loh1, S E Newey, K E Davies, D J Blake.   

Abstract

Dystrophin is the key component in the assembly and maintenance of the dystrophin-associated protein complex (DPC) in skeletal muscle. In kidney, dystroglycan, an integral component of the DPC, is involved in kidney epithelial morphogenesis, suggesting that the DPC is important in linking the extracellular matrix to the internal cytoskeleton of kidney epithelia. Here, we have investigated the molecular architecture of dystrophin-like protein complexes in kidneys from normal and dystrophin-deficient mice. Using isoform-specific antibodies, we show that the different cell types that make up the kidney maintain different dystrophin-like complexes. These complexes can be broadly grouped according to their dystrobrevin content: beta-dystrobrevin containing complexes are present at the basal region of renal epithelial cells, whilst alpha-dystrobrevin-1 containing complexes are found in endothelial and smooth muscle cells. Furthermore, these complexes are maintained even in the absence of all dystrophin isoforms. Thus our data suggest that the functions and assembly of the dystrophin-like complexes in kidney differ from those in skeletal muscle and implicate a protein other than dystrophin as the primary molecule in the assembly and maintenance of kidney complexes. Our findings also provide a possible explanation for the lack of kidney pathology in Duchenne muscular dystrophy patients and mice lacking all dystrophin isoforms.

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Year:  2000        PMID: 10893187     DOI: 10.1242/jcs.113.15.2715

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  11 in total

1.  Association of alpha-dystrobrevin with reorganizing tight junctions.

Authors:  A Sjö; K E Magnusson; K H Peterson
Journal:  J Membr Biol       Date:  2005-01       Impact factor: 1.843

Review 2.  Protein/protein interactions (PDZ) in proximal tubules.

Authors:  J Biber; S M Gisler; N Hernando; H Murer
Journal:  J Membr Biol       Date:  2005-02       Impact factor: 1.843

Review 3.  Dystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy gene.

Authors:  Ramin Tadayoni; Alvaro Rendon; L E Soria-Jasso; Bulmaro Cisneros
Journal:  Mol Neurobiol       Date:  2011-11-22       Impact factor: 5.590

4.  Renal involvement in the pathogenesis of mineral and bone disorder in dystrophin-deficient mdx mouse.

Authors:  Eiji Wada; Takayuki Hamano; Isao Matsui; Mizuko Yoshida; Yukiko K Hayashi; Ryoichi Matsuda
Journal:  J Physiol Sci       Date:  2019-05-11       Impact factor: 2.781

5.  Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1) as a dystrobrevin-binding protein.

Authors:  Ramin Nazarian; Marta Starcevic; Melissa J Spencer; Esteban C Dell'Angelica
Journal:  Biochem J       Date:  2006-05-01       Impact factor: 3.857

6.  Role of beta-dystrobrevin in nonmuscle dystrophin-associated protein complex-like complexes in kidney and liver.

Authors:  N Y Loh; D Nebenius-Oosthuizen; D J Blake; A J Smith; K E Davies
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

Review 7.  Therapeutics for Duchenne muscular dystrophy: current approaches and future directions.

Authors:  Sasha Bogdanovich; Kelly J Perkins; Thomas O B Krag; Tejvir S Khurana
Journal:  J Mol Med (Berl)       Date:  2003-12-12       Impact factor: 4.599

Review 8.  Dystroglycan: emerging roles in mammary gland function.

Authors:  M Lynn Weir; John Muschler
Journal:  J Mammary Gland Biol Neoplasia       Date:  2003-10       Impact factor: 2.673

9.  Tyrosine-phosphorylated and nonphosphorylated isoforms of alpha-dystrobrevin: roles in skeletal muscle and its neuromuscular and myotendinous junctions.

Authors:  R Mark Grady; Mohammed Akaaboune; Alexander L Cohen; Margaret M Maimone; Jeff W Lichtman; Joshua R Sanes
Journal:  J Cell Biol       Date:  2003-02-25       Impact factor: 10.539

10.  Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.

Authors:  Nellie Y Loh; Liz Bentley; Henrik Dimke; Sjoerd Verkaart; Paolo Tammaro; Caroline M Gorvin; Michael J Stechman; Bushra N Ahmad; Fadil M Hannan; Sian E Piret; Holly Evans; Ilaria Bellantuono; Tertius A Hough; William D Fraser; Joost G J Hoenderop; Frances M Ashcroft; Steve D M Brown; René J M Bindels; Roger D Cox; Rajesh V Thakker
Journal:  PLoS One       Date:  2013-01-30       Impact factor: 3.240

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