Literature DB >> 14153482

MUTANT GENES REGULATING THE INDUCIBILITY OF KYNURENINE SYNTHESIS.

T M RIZKI.   

Abstract

Alterations in the cellular synthesis of kynurenine in the larval fatbody of Drosophila melanogaster may be obtained by feeding the precursor tryptophan or by changing the genotype. In the wild type Ore-R strain, autofluorescent kynurenine globules normally occur in the cells in the anterior regions of the fatbody designated as regions 1, 2, and 3. When tryptophan is included in the larval diet, kynurenine will develop throughout the entire fatbody, thus extending to the cells in regions 4, 5, and 6. In the fatbodies of both the sepia mutant strain and the mutant combinations of the suppressible vermilion alleles with the suppressor gene (su(2)-s, v(1) and su(2)-s, v(2)), kynurenine is found in the cells from region 1 through region 4. This involvement of additional cells in the synthesis of kynurenine occurs under the usual culture conditions for Drosophila. When sepia larvae are fed tryptophan, kynurenine appears in all of the cells of the fatbody. However, dietary tryptophan does not induce kynurenine production in cells in regions 5 and 6 in the mutant combination su(2)-s, v(1) or su(2)-s, v(2). In the latter strains, an increase in the quantity of kynurenine in the fatbody is detected, but this increase remains limited to the same cells in which kynurenine production is found under normal feeding conditions. When the v(36f) allele is combined with the su(2)-s allele, an extremely faint autofluorescence characteristic of kynurenine is found in some of the anteriormost fat cells of regions 1 and 2. This autofluorescence becomes intensified when tryptophan is fed to su(2)-s, v(36f) larvae. The genetic control of kynurenine synthesis in the cells of the fatbody of Drosophila melanogaster has been previously demonstrated. The present observations establish genetic regulation of the ability to induce kynurenine production within a cell through the administration of the inducer tryptophan. Kynurenine production has been considered as a unit function of the cell as a whole rather than of the enzyme alone, and it has been concluded that even though cells in different parts of the body perform this same function (kynurenine production), the gene loci regulating this function may be different for cells in different regions of the body. A phenomenon of overlapping domains of gene actions at the cellular level offers a genetic and cellular basis for developmental and physiological homeostasis.

Entities:  

Keywords:  CHROMOSOMES; DROSOPHILA; EXPERIMENTAL LAB STUDY; KYNURENINE; LUMINESCENCE; MUTATION; TRYPTOPHAN

Mesh:

Substances:

Year:  1964        PMID: 14153482      PMCID: PMC2106435          DOI: 10.1083/jcb.21.2.203

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  7 in total

1.  Studies on tryptophan pyrrolase in Drosophila melanogaster.

Authors:  S KAUFMAN
Journal:  Genetics       Date:  1962-07       Impact factor: 4.562

2.  PSEUDO-ALLELISM AT THE VERMILION LOCUS IN DROSOPHILA MELANOGASTER.

Authors:  M M Green
Journal:  Proc Natl Acad Sci U S A       Date:  1954-02       Impact factor: 11.205

3.  A Physiological Study of the Vermilion Eye Color Mutants of Drosophila Melanogaster.

Authors:  P B Shapard
Journal:  Genetics       Date:  1960-04       Impact factor: 4.562

4.  Cytodifferentiation in the rosy mutant of Drosophila melanogaster.

Authors:  T M RIZKI; R M RIZKI
Journal:  J Cell Biol       Date:  1962-01       Impact factor: 10.539

5.  Intracellular localization of kynurenine in the fatbody of Drosophila.

Authors:  M T RIZKI
Journal:  J Biophys Biochem Cytol       Date:  1961-03

6.  FACTORS AFFECTING THE INTRACELLULAR SYNTHESIS OF KYNURENINE.

Authors:  T M RIZKI; R M RIZKI
Journal:  J Cell Biol       Date:  1964-04       Impact factor: 10.539

7.  Genetic control of cytodifferentiation.

Authors:  T M RIZKI
Journal:  J Cell Biol       Date:  1963-03       Impact factor: 10.539

  7 in total
  6 in total

1.  Adipose tissue ofDrosophila melanogaster : VI. Nonsusceptibility of the immature larval fat body to the lytic environment of the young adult.

Authors:  F M Butterworth
Journal:  Wilhelm Roux Arch Entwickl Mech Org       Date:  1973-12

2.  Molecular characterization of the Drosophila vermilion locus and its suppressible alleles.

Authors:  L L Searles; R A Voelker
Journal:  Proc Natl Acad Sci U S A       Date:  1986-01       Impact factor: 11.205

3.  Molecular cloning of suppressor of sable, a Drosophila melanogaster transposon-mediated suppressor.

Authors:  D Y Chang; B Wisely; S M Huang; R A Voelker
Journal:  Mol Cell Biol       Date:  1986-05       Impact factor: 4.272

4.  Hemocyte responses to implanted tissues inDrosophila melanogaster larvae.

Authors:  Rose M Rizki; T M Rizki
Journal:  Wilehm Roux Arch Dev Biol       Date:  1980-10

5.  Developmental analysis of a temperature-sensitive melanotic tumor mutant inDrosophila melanogaster.

Authors:  T M Rizki; Rose M Rizki
Journal:  Wilehm Roux Arch Dev Biol       Date:  1980-10

6.  Genetic regulation of Caenorhabditis elegans lysosome related organelle function.

Authors:  Alexander A Soukas; Christopher E Carr; Gary Ruvkun
Journal:  PLoS Genet       Date:  2013-10-24       Impact factor: 5.917

  6 in total

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