Environmental factors affecting the quantity of alcohol dehydrogenase in Drosophila melanogaster

Nature ◽  
1979 ◽  
Vol 280 (5722) ◽  
pp. 517-518 ◽  
Author(s):  
BRYAN CLARKE ◽  
ROBERT G. CAMFIELD ◽  
ALISON M. GALVIN ◽  
CHRISTOPHER R. PITTS
Keyword(s):  
Drosophila Melanogaster ◽  
Environmental Factors ◽  
Alcohol Dehydrogenase ◽  
Factors Affecting

scholarly journals Seasonal variation in the frequencies of the alcohol dehydrogenase isoalleles of Drosophila: correlation with environmental factors

1979 ◽  
Vol 34 (3) ◽  
pp. 317-319 ◽  
Author(s):  
Maria A. Gionfriddo ◽  
Charles L. Vigue ◽  
Pierre A. Weisgram
Keyword(s):  
Drosophila Melanogaster ◽  
Seasonal Variation ◽  
Relative Humidity ◽  
Environmental Factors ◽  
Alcohol Dehydrogenase ◽  
Seasonal Variations ◽  
Correlation Coefficients ◽  
Barometric Pressure

SUMMARYDrosophila melanogaster adults were collected throughout the summers of 1976 and 1977 in Hartford, Connecticut. The frequencies of the Adh isoalleles were determined and seasonal variation demonstrated. Correlation coefficients were calculated between Adh frequencies and the seasonal variations in temperature, precipitation, relative humidity and barometric pressure. Although five correlations were significant it was concluded that these were due to chance.

Environmental factors affecting reproducibility of bioremediation field assays in Antarctica

2020 ◽  
Vol 169 ◽  
pp. 102915 ◽  
Author(s):  
L.M. Martínez Álvarez ◽  
L.A.M. Ruberto ◽  
J.M. Gurevich ◽  
W.P. Mac Cormack
Keyword(s):  
Environmental Factors ◽  
Factors Affecting

scholarly journals The Alcohol Dehydrogenase Gene Is Nested in the outspread Locus of Drosophila melanogaster

Genetics ◽  
1996 ◽  
Vol 143 (2) ◽  
pp. 897-911 ◽  
Author(s):  
S McNabb ◽  
S Greig ◽  
T Davis
Keyword(s):  
Drosophila Melanogaster ◽  
Alcohol Dehydrogenase ◽  
Pcr Amplification ◽  
Transcription Unit ◽  
Adjacent Gene ◽  
Dehydrogenase Gene ◽  
Chromosomal Breakpoints ◽  
Splicing Patterns ◽  
Somatic Musculature

Abstract This report describes the structure and expression of the outspread (osp) gene of Drosophila melanogaster. Previous work showed that chromosomal breakpoints associated with mutations of the osp locus map to both sides of the alcohol dehydrogenase gene (Adh), suggesting that Adh and the adjacent gene Adh' are nested in osp. We extended a chromosomal walk and mapped additional osp mutations to define the maximum molecular limit of osp as 119 kb. We identified a 6-kb transcript that hybridizes to osp region DNA and is altered or absent in osp mutants. Accumulation of this RNA peaks during embryonic and pupal periods. The osp cDNAs comprise two distinct classes based on alternative splicing patterns. The 5′ end of the longest cDNA was extended by PCR amplification. When hybridized to the osp walk, the 5′ extension verifies that Adh and Adh' are nested in osp and shows that osp has a transcription unit of ≥74 kb. In situ hybridization shows that osp is expressed both maternally and zygotically. In the ovary, osp is transcribed in nurse cells and localized in the oocyte. In embryos, expression is most abundant in the developing visceral and somatic musculature.

scholarly journals GENETIC AND BIOCHEMICAL BASIS OF ENZYME ACTIVITY VARIATION IN NATURAL POPULATIONS. I. ALCOHOL DEHYDROGENASE IN DROSOPHILA MELANOGASTER

Genetics ◽  
1978 ◽  
Vol 89 (2) ◽  
pp. 371-388
Author(s):  
John F McDonald ◽  
Francisco J Ayala
Keyword(s):  
Gene Regulation ◽  
Drosophila Melanogaster ◽  
Alcohol Dehydrogenase ◽  
Natural Populations ◽  
Difficult Problem ◽  
Regulatory Genes ◽  
Biochemical Basis ◽  
Evolutionary Consequence ◽  
The Third ◽  
Adh Activity

ABSTRACT Recent studies by various authors suggest that variation in gene regulation may be common in nature, and might be of great evolutionary consequence; but the ascertainment of variation in gene regulation has proven to be a difficult problem. In this study, we explore this problem by measuring alcohol dehydrogenase (ADH) activity in Drosophila melanogaster strains homozygous for various combinations of given second and third chromosomes sampled from a natural population. The structural locus (Adh) coding for ADH is on the second chromosome. The results show that: (1) there are genes, other than Adh, that affect the levels of ADH activity; (2) at least some of these "regulatory" genes are located on the third chromosome, and thus are not adjacent to the Adh locus; (3) variation exists in natural populations for such regulatory genes; (4) the effect of these regulatory genes varies as they interact with different second chromosomes; (5) third chromosomes with high-activity genes are either partially or completely dominant over chromosomes with low-activity genes; (6) the effects of the regulatory genes are pervasive throughout development; and (7) the third chromosome genes regulate the levels of ADH activity by affecting the number of ADH molecules in the flies. The results are consistent with the view that the evolution of regulatory genes may play an important role in adaptation.

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