TY - JOUR
T1 - Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle
AU - Jurynec, Michael J.
AU - Xia, Ruohong
AU - Mackrill, John J.
AU - Gunther, Derrick
AU - Crawford, Thomas
AU - Flanigan, Kevin M.
AU - Abramson, Jonathan J.
AU - Howard, Michael T.
AU - Grunwald, David Jonah
PY - 2008/8/26
Y1 - 2008/8/26
N2 - Mutations affecting the seemingly unrelated gene products, SepN1, a selenoprotein of unknown function, and RyR1, the major component of the ryanodine receptor intracellular calcium release channel, result in an overlapping spectrum of congenital myopathies. To identify the immediate developmental and molecular roles of SepN and RyR in vivo, loss-of-function effects were analyzed in the zebrafish embryo. These studies demonstrate the two proteins are required for the same cellular differentiation events and are needed for normal calcium fluxes in the embryo. SepN is physically associated with RyRs and functions as a modifier of the RyR channel. In the absence of SepN, ryanodine receptors from zebrafish embryos or human diseased muscle have altered biochemical properties and have lost their normal sensitivity to redox conditions, which likely accounts for why mutations affecting either factor lead to similar diseases.
AB - Mutations affecting the seemingly unrelated gene products, SepN1, a selenoprotein of unknown function, and RyR1, the major component of the ryanodine receptor intracellular calcium release channel, result in an overlapping spectrum of congenital myopathies. To identify the immediate developmental and molecular roles of SepN and RyR in vivo, loss-of-function effects were analyzed in the zebrafish embryo. These studies demonstrate the two proteins are required for the same cellular differentiation events and are needed for normal calcium fluxes in the embryo. SepN is physically associated with RyRs and functions as a modifier of the RyR channel. In the absence of SepN, ryanodine receptors from zebrafish embryos or human diseased muscle have altered biochemical properties and have lost their normal sensitivity to redox conditions, which likely accounts for why mutations affecting either factor lead to similar diseases.
KW - Congenital myopathy
KW - Disease model
KW - Intracellular calcium release
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U2 - 10.1073/pnas.0806015105
DO - 10.1073/pnas.0806015105
M3 - Article
C2 - 18713863
AN - SCOPUS:50449088082
SN - 0027-8424
VL - 105
SP - 12485
EP - 12490
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 34
ER -