Molecular Biology and Evolution, Vol 9, 526-536, Copyright © 1992 by Society for Molecular Biology and Evolution
P Matthew, A Agrotis, AC Taylor and SW McKechnie
Southern analysis of the Adh region of 212 Drosophila melanogaster lines
collected from the Tahbilk winery revealed linkage disequilibrium between a
37-bp insertion [designated delta 2 by Kreitman (1983)] and the fast
electrophoretic variant of alcohol dehydrogenase (ADH-F). Among these lines
34% contained the insert and encoded ADH-F, 33.5% encoded ADH-F and did not
have the insert, and 32.5% encoded the slow electrophoretic variant of
alcohol dehydrogenase (ADH-S). Strong linkage association between this
insert and ADH-F is evident worldwide. Twenty-nine of the second chromosome
lines were characterized for ADH protein quantity by using radial
immunodiffusion. ADH quantity was estimated in both larvae and adult males
raised in the presence and absence of alcohol supplement to each of two
different food media. Analyses of variance indicated higher levels of ADH
protein in larvae from lines with the insert (all ADH-F), compared with
those without (both ADH-F and ADH-S), independent of either dietary alcohol
or media type. No such difference in ADH quantity between insert- and
noninsert- containing ADH-F lines was detected in adults, although the
expected higher levels occurred in ADH-F lines compared with ADH-S lines.
Given the high levels of linkage disequilibrium in the Adh region, these
data suggest that either polymorphic nucleotide-site variants positively
associated with delta 2 on the second chromosome or delta 2 itself
increases larval levels of ADH protein.
ORIGINAL ARTICLE
An association between ADH protein levels and polymorphic nucleotide variation in the Adh gene of Drosophila melanogaster
Department of Genetics and Developmental Biology, Monash University, Clayton, Victoria, Australia.
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