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PMID: 6788034 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Genetic and functional analysis of tryptophan transport in Malpighian tubules of Drosophila.

Biochemical genetics ·Vol. 18 ·No. 11-12 ·1980-12-00 ·Pages 1109-30

Sullivan DT, Bell LA, Paton DR, Sullivan MC

Abstract

Dissected Malpighian tubules from wild type and the eye color mutant white of Drosophila were compared with respect to their abilities to transport tryptophan and kynurenine into tubule cells. It was determined that mutation at white greatly impairs the ability of Malpighian tubule cells to take up tryptophan. Functional studies on the extracellular spaces and ultrastructural observations indicated no differences in these respects between wild type and white tubules. It is consistent with several observations that much of the tryptophan associated with white exists in the intercellular spaces. Furthermore, the uptake of tryptophan by the w+ system of wild type tubules is inhibited by the analogue 5-methyl-tryptophan. However, the incorporation of radioactive tryptophan into protein in tubule cells from wild type and white occurs at the same rates and is not affected by 5-methyl-tryptophan. Therefore, it is apparent that Malpighian tubules have a transport system that enables entry of tryptophan into a cellular pool and that this cellular pool is initially independent of the tryptophan pool used for protein synthesis. The mutant white lacks this transport system. From these studies and others it appears that compartmentalization of cellular pools may be brought about via the utilization of specific membrane transport systems.

MeSH Terms
Animals Biological Transport, Active Cloaca/metabolism Drosophila melanogaster/genetics Female Malpighian Tubules/metabolism Mutation Phenotype Tryptophan/genetics,metabolism
Chemicals
Tryptophan
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sullivan D T
Bell L A
Paton D R
Sullivan M C
References (13)
13 references, click to expand
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Article Info
Journal
Biochemical genetics
Abbr.
Biochem Genet
ISSN
0006-2928
Published
1980-12-00
Pages
1109-30
Language
English
Region
United States
NLM ID
0126611
Subset
IM
Grants
NIGMS NIH HHS · GM 22366 · United States
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