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PMID: 2499511 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Developmental genetics of loci at the base of the X chromosome of Drosophila melanogaster.

Genetics ·Vol. 121 ·No. 2 ·1989-02-00 ·Pages 313-31

Perrimon N, Smouse D, Miklos GL

Abstract

We have conducted a genetic and developmental analysis of the 26 contiguous genetic complementation groups within the 19D3-20F2 interval of the base of the X chromosome, a region of 34 polytene bands delimited by the maroon-like and suppressor of forked loci. Within this region there are four loci which cause visible phenotypes but which have little or no effect on zygotic viability (maroon-like, little fly, small optic lobes and sluggish). There are 22 loci which, when mutated, are zygotic lethals and three of these, legless/runt, folded gastrulation and 13E3, have severe effects on embryonic development. In addition, three visible phenotypes have been defined only by overlapping deficiencies (melanized-like, tumorous head, and varied outspread). We have analyzed the lethal phases and maternal requirement of 58 mutations at 22 of the zygotic lethal loci by means of germline clone analysis using the dominant female sterile technique. Additionally, all lethal complementation groups, as well as a specific subset of deficiencies, have been studied histologically for defects in the development of the central and peripheral embryonic nervous systems.

MeSH Terms
Animals Chromosome Mapping Drosophila melanogaster/embryology,genetics Female Gastrula/physiology Genes, Lethal Genetic Complementation Test Germ Cells Nervous System/embryology Phenotype Suppression, Genetic X Chromosome/ultrastructure
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Perrimon N
Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02115.
Smouse D
Miklos G L
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Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1989-02-00
Pages
313-31
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1203620
Subset
IM
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