Molecular cloning of a functional allatostatin gut/brain receptor and an allatostatin preprohormone from the silkworm Bombyx mori

J Biol Chem. 2001 Dec 14;276(50):47052-60. doi: 10.1074/jbc.M106675200. Epub 2001 Oct 4.

Abstract

The cockroach-type or A-type allatostatins are inhibitory insect neuropeptides with the C-terminal sequence Tyr/Phe-X-Phe-Gly-Leu-NH(2). Here, we have cloned an A-type allatostatin receptor from the silkworm Bombyx mori (BAR). BAR is 361 amino acid residues long, has seven transmembrane domains, shows 60% amino acid residue identity with the first Drosophila allatostatin receptor (DAR-1), and 48% identity with the second Drosophila allatostatin receptor (DAR-2). The BAR gene has two introns and three exons. These two introns coincide with and have the same intron phasing as two introns in the DAR-1 and DAR-2 genes, showing that the three receptors are not only structurally but also evolutionarily related. Furthermore, we have cloned a Bombyx allatostatin preprohormone that contains eight different A-type allatostatins. Chinese hamster ovary cells permanently transfected with BAR DNA react on the addition of 4 x 10(-9)M Bombyx A-type allatostatins with a second messenger cascade (measured as bioluminescence), showing that BAR is a functional A-type allatostatin receptor. Southern blots suggest that Bombyx has at least one other BAR-related gene in addition to the BAR gene described in this paper. Northern blots and quantitative reverse transcriptase-polymerase chain reaction of different larval tissues show that BAR mRNA is mainly expressed in the gut and to a much lesser extent in the brain. To our knowledge, this is the first report on the molecular cloning and functional expression of an insect gut/brain peptide hormone receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Blotting, Northern
  • Blotting, Southern
  • Bombyx
  • Brain / metabolism*
  • CHO Cells
  • Cloning, Molecular
  • Cricetinae
  • DNA, Complementary / metabolism
  • Digestive System / metabolism*
  • Dose-Response Relationship, Drug
  • Drosophila
  • Drosophila Proteins*
  • Evolution, Molecular
  • Exons
  • Hormones / genetics*
  • Insect Proteins*
  • Introns
  • Kinetics
  • Molecular Sequence Data
  • Neuropeptides*
  • Phylogeny
  • Protein Precursors / genetics*
  • RNA, Messenger / metabolism
  • Receptors, Cell Surface / chemistry*
  • Receptors, Cell Surface / genetics*
  • Receptors, Cell Surface / metabolism*
  • Receptors, G-Protein-Coupled*
  • Receptors, Neuropeptide*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • Tissue Distribution
  • Transfection

Substances

  • AstA-R1 protein, Drosophila
  • AstA-R2 protein, Drosophila
  • DNA, Complementary
  • Drosophila Proteins
  • Hormones
  • Insect Proteins
  • Neuropeptides
  • Protein Precursors
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, G-Protein-Coupled
  • Receptors, Neuropeptide

Associated data

  • GENBANK/AF254742
  • GENBANK/AF303368
  • GENBANK/AF303369
  • GENBANK/AF303370
  • GENBANK/AF309090