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Open AccessJournal ArticleDOI

The genetics of a small chromosome region of Drosophila melanogaster containing the structural gene for alcohol dehydrogenase. IV: scutoid, an antimorphic mutation.

Michael Ashburner, +2 more
- 01 Nov 1982 - 
- Vol. 102, Iss: 3, pp 401-420
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TLDR
The simplest hypothesis is that Sco is a small reciprocal transposition, the genes noc, osp, and Adh exchanging places with three genes normally mapping proximal to them: l(2)br34, 1( 2)br35 and rd.
Abstract
Exchange mapping locates the dominant mutation Scutoid to the right of Adh on chromosome arm 2L of D. melonogoster. However, deletion mapping indicates that Sco is to the left of Adh. The phenotype of Sco is sensitive to mutation, or deletion, of noc+ and of three genes, el, l(Z)br22, and l(2)br29 mapping immediately distal to noc. The four contiguous loci, el, 1(2)br22, l(2) br29 and noc, although separable by deletion end points, interact, because certain (or all) alleles of these four loci show partial failure of complementation, or even negative complementation. The simplest hypothesis is that Sco is a small reciprocal transposition, the genes noc, osp, and Adh exchanging places with three genes normally mapping proximal to them: 1(2)br34,1(2)br35 and rd. The Sco phenotype is thought to result from a position effect at the newly created noc/l(2)br28 junction. APPING close to the structural gene for alcohol dehydrogenase (Adh) on M chromosome arm 2L of Drosophila melanogaster is the dominant mutation Scutoid (Sco). This mutation was induced with X rays by KRIVSHENKO (1959) and, when heterozygous, results in a specific pattern of loss of bristles from the head and thorax of the adult fly. The map location of Sco made it an obvious marker to use for the genetic analysis of Adh and for the analysis of the genetic structure of the environs of Adh. It soon became apparent, however, that Sco is a rather exceptional mutation. For example, the map position of Sco determined by recombination and that determined by deletion analysis are contradictory. Moreover, Sco, although normally a stable mutation, can be reverted by X rays at a high frequency. Analysis of the revertants of Sco revealed an unexpected genetic complexity in the structure of the Sco chromosome. This and a following paper (M. ASHBURNER et al., unpublished results) are devoted to a genetic analysis of Sco and its revertants. It will probably help the reader if we begin by summarizing the structure of the Sco mutation that we consider the data warrant. MODEL

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Maternal-effect mutations altering the anterior-posterior pattern of the Drosophila embryo.

TL;DR: Analysis of embryos derived from double mutant mothers suggests that these three phenotypic groups of mutants interfere with three different, independent pathways, which seem to act additively on the system which specifies anterior-posterior cellular fates within the egg.
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Posterior localization of vasa protein correlates with, but is not sufficient for, pole cell development.

TL;DR: It is indicated that vasa protein, when properly localized, is not sufficient for induction of pole cell development, and that at least the tudor and valois wild-type functions are also required specifically for this process.
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Maternal-zygotic gene interactions during formation of the dorsoventral pattern in drosophila embryos

TL;DR: A zygotic action for the dl gene in addition to the maternal effect was revealed by the finding that extra doses of dl(+) in the zygotes can partially rescue the dominant lethality ofheterozygous twi embryos derived from heterozygous dl females at high temperature.
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Cadherin-mediated cell adhesion and cell motility in Drosophila trachea regulated by the transcription factor Escargot

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References
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Journal ArticleDOI

The genetics of a small autosomal region of Drosophila melanogaster containing the structural gene for alcohol dehydrogenase. II. Lethal mutations in the region.

TL;DR: Lethals mapping close to the structural gene for alcohol dehydrogenase, both distally and proximally, have been identified and will be used for the construction of selective crosses for the study of exchange within this locus.
Journal ArticleDOI

The genetics of a small autosomal region of drosophila melanogaster containing the structural gene for alcohol dehydrogenase. i. characterization of deficiencies and mapping of adh and visible mutations

TL;DR: The position of the structural gene coding for alcohol dehydrogenase (ADH) in Drosophila melanogaster has been shown to be within polytene chromosome bands 35B1 and 35B3, most probably within 35B2.
Journal ArticleDOI

Genetic and cytogenetic analysis of the Adh region in Drosophila melanogaster.

TL;DR: Eighteen Adh-negative mutations were selected with 1-pentyn-3-ol after feeding of formaldehyde and Twelve of the 18 were shown by cytological and genetic analysis to be deletions, allowing us to localize the Adh gene to a region including bands 35B3-5 on the left arm of chromosome 2.
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