Alternative promoter usage generates multiple evolutionarily conserved isoforms of Drosophila DOA kinase

Genesis. 2008 Mar;46(3):132-43. doi: 10.1002/dvg.20374.

Abstract

The unique LAMMER (or Clk) protein kinase of Drosophila is encoded at the Doa locus. To better understand the pleiotropic effects of Doa mutations, we describe the structure and expression of the multiple RNA and protein products of the locus, as well as their evolutionary conservation among Drosophila. The gene produces at least six different protein isoforms, primarily through alternative promoter usage, generating kinases with virtually identical catalytic domains but variable N-terminal noncatalytic domains. The single known alternative splicing event generates a kinase with the insertion of six additional amino-acids in the catalytic domain. Two independent predicted genes nested within Doa introns actually encode additional alternative N-termini of the locus. An alternative polyadenylation site utilized exclusively during early embryogenesis generates a transcript with a short half-life, apparently to ensure a "burst" of kinase expression at the onset of development. Ecdysone induction of Doa transcripts affects all isoforms during pupariation. Finally, extensive conservation of amino-acid sequences of both the catalytic and N-terminal noncatalytic exons observed in alignments between D. melanogaster exons and the genome sequences of 11 other Drosophila species suggest that the multiple isoforms serve important and nonredundant functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • 3' Untranslated Regions / physiology
  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Conserved Sequence*
  • Drosophila / enzymology
  • Drosophila / genetics*
  • Drosophila / growth & development
  • Drosophila Proteins / genetics*
  • Ecdysone / pharmacology
  • Embryo, Nonmammalian
  • Evolution, Molecular*
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Enzymologic / drug effects
  • Isoenzymes / drug effects
  • Isoenzymes / genetics
  • Promoter Regions, Genetic / physiology*
  • Protein Serine-Threonine Kinases / genetics*
  • Pupa / enzymology
  • Pupa / genetics
  • RNA, Messenger / metabolism

Substances

  • 3' Untranslated Regions
  • Drosophila Proteins
  • Isoenzymes
  • RNA, Messenger
  • Ecdysone
  • Doa protein, Drosophila
  • Protein Serine-Threonine Kinases