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Mutations in the protein phosphatase 1 gene at 87B can differentially affect suppression of position-effect variegation and mitosis in Drosophila melanogaster.
Author(s) -
Katalin Baksa,
Henning Morawietz,
Viktor Dombrádi,
Myles Axton,
Hans Taubert,
Gábor Szabó,
I. Török,
Andor Udvardy,
Henrik Gyurkovics,
Balázs Szöőr
Publication year - 1993
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/135.1.117
Subject(s) - biology , genetics , locus (genetics) , drosophila melanogaster , mitosis , complementation , variegation (histology) , position effect , mutant , gene , allele , mitotic crossover , protein fragment complementation assay , phenotype , microbiology and biotechnology
The suppressor of position effect variegation (PEV) locus Su-var(3)6 maps to 87B5-10. The breakpoints of deficiencies that define this interval have been placed on a 250-kb molecular map of the region. The locus is allelic to the ck19 complementation group previously shown to encode a type 1 serine-threonine protein phosphatase (PP1) catalytic subunit. When introduced into flies by P element-mediated transformation, a 5.8-kb genomic fragment carrying this gene overcomes the suppressor phenotype of Su-var(3)6(01) and recessive lethality of all mutations of the locus. Four of the mutant alleles at the locus show a broad correlation between high levels of suppression of PEV, a high frequency of aberrant mitosis and low PP1 activity in larval extracts. However, some alleles with low PP1 activity show weak suppression of PEV with a high frequency of abnormal mitosis, whereas others show strong suppression of PEV with normal mitosis. The basis for these discussed.

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