In this report we describe the developmental expression of the murine
(Mobp) gene encoding myelin-associated oligodendrocytic basic protein.
We have characterized three Mobp cDNA clones which have been used as
probes. Murine Mobp splice variant-1 (mmsv-1), a portion of 3' untrans
lated region (UTR), is homologous to 3' UTR sequences found in the rat
Mobp splice variants rOP1, Mobp81-A and Mobp-99. The mmsv-2 sequence,
encoding 81 amino acids, closely resembles the rat Mobp81-A splice va
riant. The mmsv-3 cDNA, encoding 170 amino acids corresponding closely
to the rat rOPRP1 splice variant, detects a single mRNA species prese
nt in low levels from E12 onward, suggesting this MOBP may have a func
tion alternative or additional to involvement in myelin formation. The
mmsv-1 probe detects an mRNA species abundantly expressed in the post
natal central nervous system (CNS) but barely detectable at E18. This
mRNA is located initially in the cell bodies of oligodendrocytes, movi
ng distally into their processes as myelination proceeds. The most abu
ndant mmsv(s) in the adult CNS are present at detectable levels after
expression of the myelin basic protein (Mbp) gene and marginally after
or coincident with the proteolipid protein (Pip) gene. The level of t
he abundant, late-expressed mRNA correlates closely with the capacity
to form myelin and the maturity of oligodendrocytes, as shown in two h
ypomyelinated mutants, rumpshaker and jimpy, which represent mildly an
d severely affected phenotypes, respectively. (C) 1997 Wiley-Liss, Inc
.