M. Misago et al., MOLECULAR-CLONING AND EXPRESSION OF CDNAS ENCODING HUMAN ALPHA-MANNOSIDASE-II AND A PREVIOUSLY UNRECOGNIZED ALPHA-MANNOSIDASE-IIX ISOZYME, Proceedings of the National Academy of Sciences of the United Statesof America, 92(25), 1995, pp. 11766-11770
Golgi alpha-mannosidase II (alpha-MII) is an enzyme involved in the pr
ocessing of N-Linked glycans. Using a previously isolated murine cDNA
clone as a probe,,ve have isolated cDNA clones encompassing the human
alpha-MII cDNA open reading frame and initiated isolation of human gen
omic clones. During the isolation of genomic clones, genes related to
that encoding alpha-MII were isolated, One such gene was found to enco
de an isozyme, designated alpha-MII(x). A 5-kb cDNA clone encoding alp
ha-MII(x) was then isolated from a human melanoma cDNA library, Howeve
r, comparison between alpha-MII(x) and alpha-MII cDNAs suggested that
the cloned cDNA encodes a truncated polypeptide with 796 amino acid re
sidues, while alpha-MII consists of 1144 amino acid residues. To reeva
luate the sequence of alpha-MII(x) cDNA, polymerase chain reaction (PC
R) was performed with lymphocyte mRNAs, Comparison of the sequence of
PCR products with the alpha-MII(x) genomic sequence revealed that alte
rnative splicing of the alpha-MII(x) transcript can result in an addit
ional transcript encoding a 1139-amino acid polypeptide. Northern anal
ysis showed transcription of alpha-MII(x) in various tissues, suggesti
ng that the alpha-MII(x) gene is a housekeeping gene. COS cells transf
ected with alpha-MII(x) cDNA containing the full-length open reading f
rame shelved an increase of alpha-mannosidase activity, The alpha-MII(
x) gene was mapped to human chromosome 15q25, whereas the alpha-MII ge
ne was mapped to 5q21-22.