A high proportion of genes involved in position effect variegation also affect chromosome inheritance

Chromosoma. 2004 Mar;112(6):269-76. doi: 10.1007/s00412-003-0272-2. Epub 2004 Feb 6.

Abstract

Suppressors and enhancers of position effect variegation (PEV) have been linked to the establishment and maintenance of heterochromatin. The presence of centromeres and other inheritance elements in heterochromatic regions suggests that suppressors and enhancers of PEV, Su(var) s and E(var)s [collectively termed Mod(var)s], may be required for chromosome inheritance. In order to test this hypothesis, we screened 59 ethyl methanesulfonate-generated Drosophila Mod(var)s for dominant effects on the partially compromised inheritance of a minichromosome ( J21A) missing a portion of the genetically defined centromere. Nearly half of these Mod(var)s significantly increased or decreased the transmission of J21A. Analyses of homozygous mutant larval neuroblasts suggest that these mutations affect cell cycle progression and native chromosome morphology. Five out of six complementation groups tested displayed mitotic abnormalities, including phenotypes such as telomere fusions, overcondensed chromosomes, and low mitotic index. We conclude that Mod(var)s as a group are highly enriched for genes that encode essential inheritance functions. We propose that a primary function of Mod(var)s is to promote chromosome inheritance, and that the gene silencing phenotype associated with PEV may be a secondary consequence of the heterochromatic structures required to carry out these functions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Cycle
  • Centromere
  • Disease Transmission, Infectious
  • Drosophila melanogaster / genetics*
  • Ethyl Methanesulfonate / toxicity
  • Female
  • Gene Silencing
  • Genes, Dominant / physiology*
  • Genes, Insect*
  • Genetic Complementation Test
  • Heterochromatin / genetics*
  • Homozygote
  • Larva / metabolism
  • Male
  • Mitotic Index
  • Mutation
  • Neurons / cytology*
  • Neurons / metabolism
  • Phenotype
  • Suppression, Genetic
  • Telomere / metabolism

Substances

  • Heterochromatin
  • Ethyl Methanesulfonate