Yw. Zheng et Mr. Felder, GENETIC-MAPPING OF A POSSIBLE NEW ALCOHOL-DEHYDROGENASE SEQUENCE TO MOUSE CHROMOSOME-3 AT THE ADH-1 ADH-3 COMPLEX/, Biochemical genetics, 35(3-4), 1997, pp. 105-117
Southern blot analysis of mouse genomic DNA reveals two EcoRI fragment
s which faintly hybridize to mouse Adh-l cDNA and are not part of the
Adh-1 gene, These fragments were isolated from agarose gels, cloned an
d characterized. Sequence analysis of the 2.1-kb EcoRI fragment sugges
ts that it is likely a pseudogene since it does not contain a long ope
n reading frame. However; the 2.0-kb EcoRI fragment contains a coding
sequence with a long open reading frame which corresponds to exon 6 of
the mouse Adh-l gene. Comparison of the coding sequence with other kn
own ADHs suggests that the sequence has diverged sufficiently from any
currently known class of ADH to be a possible distinct class. Further
confirmation, awaits analysis of currently available genomic clones.
Using these sequences as probe, restriction fragment length polymorphi
sms were identified for each sequence between C57B1/6J and DBA/2J inbr
ed mouse strains, The strain distribution pattern for these allelic di
fferences was determined among the B x D recombinant inbred strains. T
his analysis revealed that the 2.1-kb EcoRI sequence is located on chr
omosome 3 but at a distance from the Adh-1/Adh-3 complex as previously
reported. However the new polymorphism identified in the 2.0-kb EcoRI
fragment enabled this sequence to be mapped at the Adh-1/Adh-3 comple
x.