Ja. Airey et al., FAILURE TO MAKE NORMAL ALPHA-RYANODINE RECEPTOR IS AN EARLY EVENT ASSOCIATED WITH THE CROOKED NECK DWARF (CN) MUTATION IN CHICKEN, Developmental dynamics, 197(3), 1993, pp. 169-188
We have investigated the molecular basis of the Crooked Neck Dwarf (cn
) mutation in embryonic chickens. Using biochemical and pharmacologica
l techniques we are unable to detect normal alpha ryanodine receptor (
RyR) protein in intact cn/cn skeletal muscle. Extremely low levels of
alphaRyR immunoreactivity can be observed in mutant muscles, but the d
istribution of this staining differs from that in normal muscle and co
localizes with the rough endoplasmic reticulum immunoglobulin binding
protein, BiP. This suggests the existence of an abnormal alphaRyR prot
ein in mutant muscle. In day E12 cn/cn muscle the levels of RyR mRNA a
re reduced by approximately 80%, while the levels of other muscle prot
eins, including the alpha1 subunit of the dihydropyridine receptor, th
e SR Ca2+-ATPase, calsequestrin, and glyceraldehyde-3-phosphate dehydr
ogenase, and their associated mRNAs are essentially normal in cn/cn mu
scle. There is also a failure to express alphaRyR in cn/cn cerebellar
Purkinje neurons. Expression of the betaRyR, a second RyR isoform, is
not initiated in normal skeletal muscle until day E18. In cn/cn skelet
al muscle significant muscle degeneration has occurred by this time an
d the betaRyR is found at low levels in only a subset of fibers sugges
ting the reduced levels of this isoform are a secondary consequence of
the mutation. The cardiac RyR isoform is found in cn/cn cardiac muscl
e, which contracts in a vigorous manner. In summary, a failure to make
normal alphaRyR receptor appears to be an event closely associated wi
th the cn mutation and one which may he largely responsible for develo
pment of the cn/cn phenotype in embryonic skeletal muscle. (C) 1993 Wi
ley-Liss, Inc.