A comparative genomic analysis of the calcium signaling machinery in Neurospora crassa, Magnaporthe grisea, and Saccharomyces cerevisiae

Fungal Genet Biol. 2004 Sep;41(9):827-41. doi: 10.1016/j.fgb.2004.05.001.

Abstract

A large number of Ca2+ -signaling proteins have been previously identified and characterized in Saccharomyces cerevisiae but relatively few have been discovered in filamentous fungi. In this study, a detailed, comparative genomic analysis of Ca2+ -signaling proteins in Neurospora crassa, Magnaporthe grisea, and S. cerevisiae has been made. Our BLAST analysis identified 48, 42, and 40 Ca2+ -signaling proteins in N. crassa, M. grisea, and S. cerevisiae, respectively. In N. crassa, M. grisea, and S. cerevisiae, 79, 100, and 13% of these proteins, respectively, were previously unknown. For N. crassa, M. grisea, and S. cerevisiae, respectively, we have identified: three Ca2+ -permeable channels in each species; 9, 12, and 5 Ca2+/cation-ATPases; eight, six, and four Ca2+ -exchangers; four, four, and two phospholipase C's; one calmodulin in each species; and 23, 21, and 29 Ca2+/calmodulin-regulated proteins. Homologs of a number of key proteins involved in the release of Ca2+ from intracellular stores, and in the sensing of extracellular Ca2+, in animal and plant cells, were not identified. The greater complexity of the Ca2+ -signaling machinery in N. crassa and M. grisea over that in S. cerevisiae probably reflects their more complex cellular organization and behavior, and the greater range of external signals which filamentous fungi have to respond to in their natural habitats. To complement the data presented in this paper, a comprehensive web-based database resource (http://www.fungalcell.org/fdf/) of all Ca2+ -signaling proteins identified in N. crassa, M. grisea, and S. cerevisiae has been provided.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcineurin / genetics
  • Calcium Channels / genetics
  • Calcium Signaling / genetics*
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Calcium-Transporting ATPases / genetics
  • Calmodulin / genetics
  • Computational Biology*
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Genes, Fungal
  • Genome, Fungal*
  • Magnaporthe / genetics*
  • Magnaporthe / metabolism
  • Models, Molecular
  • Neurospora crassa / genetics*
  • Neurospora crassa / metabolism
  • Phylogeny
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / metabolism
  • Sequence Homology
  • Sodium-Calcium Exchanger / genetics
  • Type C Phospholipases / genetics

Substances

  • Calcium Channels
  • Calmodulin
  • Fungal Proteins
  • Sodium-Calcium Exchanger
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Calcineurin
  • Type C Phospholipases
  • Calcium-Transporting ATPases