Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P51532 (
transcriptional activator
)
6,546
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
p94
/
calpain 3
is a skeletal muscle-specific member of the Ca(2+)-regulated cytosolic cysteine protease family, the calpains. Defective
p94
protease activity originating from gene mutations causes a muscular dystrophy called calpainopathy, indicating the indispensability of
p94
for muscle survival. Because of the existence of the
p94
-specific regions IS1 and IS2,
p94
undergoes very rapid and exhaustive autolysis. To elucidate the physiological relevance of this unique activity, the autolytic profiles of
p94
and the effect of the
p94
binding protein, connectin/titin, on this process were investigated. In vitro analysis of
p94
autolysis showed that autolysis in IS1 proceeds without immediate disassembly into fragments and that the newly identified cryptic autolytic site in IS2 is critical for disassembling autolyzed fragments. As a genetic system to assay
p94
autolysis semiquantitatively,
p94
was expressed in yeast as a hybrid protein between the DNA binding and activation domains of the yeast
transcriptional activator
Gal4. Transcriptional activation by the Gal4-
p94
:WT hybrid protein is precluded by
p94
autolysis. Complete or partial loss of autolytic activity by C129S active site mutation, limb girdle muscular dystrophy type 2A pathogenic missense mutations, or PCR-based random mutagenesis could be detected by semiquantitative restoration of Gal4-dependent beta-galactosidase gene expression. Using this system, the N2A connectin fragment that binds to
p94
was shown to suppress
p94
autolytic disassembly. The proximity of the IS2 autolytic and connectin-binding sites in
p94
suggested that N2A connectin suppresses IS2 autolysis. These data indicate the importance of
p94
-connectin interaction in the control of
p94
functions by regulating autolytic decay of
p94
.
...
PMID:Suppressed disassembly of autolyzing p94/CAPN3 by N2A connectin/titin in a genetic reporter system. 1662 76