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PMID: 6785043 Published · ppublish English Journal Article

An RNA polymerase II mutation in Drosophila melanogaster that mimics ultrabithorax.

Chromosoma ·Vol. 82 ·No. 2 ·1981-00-00 ·Pages 237-47

Mortin MA, Lefevre G

Abstract

An EMS-induced, sex-linked recessive lethal mutation that in heterozygous condition mimics the third-chromosome dominant mutant Ultrabithorax-130 (Ubx130) has been discovered in Drosophila melanogaster. This Ultrabithorax-like (Ubl) mutant, when heterozygous, adds several hairs to and enlarges the apical segment (capitellum) of the haltere. Ubl fails to complement Ubln [previously called l (1) L5], a recessive lethal null allele located in section 10C of Bridges' (1938) map of the polytene X chromosome at map position 35.7 Ubl behaves as an antimorph: heterozygous deficiencies for section 10C do not display the Ubl dominant phenotype. Ubl shows a dosage effect: the maximum expression occurs in females with the genotype Ubl/Ubl; Dp Ubl+, in which the capitellum is about three times as large as that of Ubl/+, with two or more rows of bristles. These flies are poorly viable and sterile when mated to Ubl; Dp Ubl+ males, but produce a few offspring when mated to Ubl+ males. Ubl displays a complex series of interactions with loci other than Ubx and elicits expression of specific mutant phenotypes when it is heterozygous in trans with certain nonallelic deficiencies and recessive mutations. Greenleaf et al. (1980) have demonstrated thatUbl is allelic with an alpha-amanitin-resistant mutation that effects RNA polymerase II; therefore, the interactions observed between Ubl and other loci may result from an inability of heterozygous Ubl flies to undergo normal transcription.

MeSH Terms
Alleles Animals DNA-Directed RNA Polymerases/genetics Drosophila melanogaster/embryology,enzymology,genetics Genetic Complementation Test Genotype Mutation Phenotype RNA Polymerase II/genetics Thorax
Chemicals
RNA Polymerase II DNA-Directed RNA Polymerases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Mortin M A
Lefevre G
References (9)
9 references, click to expand
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Article Info
Journal
Chromosoma
Abbr.
Chromosoma
ISSN
0009-5915
Published
1981-00-00
Pages
237-47
Language
English
Region
Austria
NLM ID
2985138R
Subset
IM
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