Crustacean hyperglycaemic hormone (CHH)-like peptides and CHH-precursor-related peptides from pericardial organ neurosecretory cells in the shore crab, Carcinus maenas, are putatively spliced and modified products of multiple genes

Biochem J. 2001 May 15;356(Pt 1):159-70. doi: 10.1042/0264-6021:3560159.

Abstract

About 24 intrinsic neurosecretory neurons within the pericardial organs (POs) of the crab Carcinus maenas produce a novel crustacean hyperglycaemic hormone (CHH)-like peptide (PO-CHH) and two CHH-precursor-related peptides (PO-CPRP I and II) as identified immunochemically and by peptide chemistry. Edman sequencing and MS revealed PO-CHH as a 73 amino acid peptide (8630 Da) with a free C-terminus. PO-CHH and sinus gland CHH (SG-CHH) share an identical N-terminal sequence, positions 1-40, but the remaining sequence, positions 41-73 or 41-72, differs considerably. PO-CHH may have different precursors, as cDNA cloning of PO-derived mRNAs has revealed several similar forms, one exactly encoding the peptide. All PO-CHH cDNAs contain a nucleotide stretch coding for the SG-CHH(41-76) sequence in the 3'-untranslated region (UTR). Cloning of crab testis genomic DNA revealed at least four CHH genes, the structure of which suggest that PO-CHH and SG-CHH arise by alternative splicing of precursors and possibly post-transcriptional modification of PO-CHH. The genes encode four exons, separated by three variable introns, encoding part of a signal peptide (exon I), the remaining signal peptide residues, a CPRP, the PO-CHH(1-40)/SG-CHH(1-40) sequences (exon II), the remaining PO-CHH residues (exon III) and the remaining SG-CHH residues and a 3'-UTR (exon IV). Precursor and gene structures are more closely related to those encoding related insect ion-transport peptides than to penaeid shrimp CHH genes. PO-CHH neither exhibits hyperglycaemic activity in vivo, nor does it inhibit Y-organ ecdysteroid synthesis in vitro. From the morphology of the neurons it seems likely that novel functions remain to be discovered.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Amino Acid Sequence
  • Animals
  • Arthropod Proteins
  • Base Sequence
  • Biological Assay
  • Blood Glucose / metabolism
  • Brachyura
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Ecdysteroids
  • Hemolymph
  • Invertebrate Hormones / genetics
  • Invertebrate Hormones / isolation & purification*
  • Male
  • Models, Genetic
  • Molecular Sequence Data
  • Neurons / chemistry*
  • Neurosecretory Systems / chemistry*
  • Peptides / genetics
  • Peptides / isolation & purification*
  • Protein Precursors / genetics
  • Protein Precursors / isolation & purification*
  • Sequence Analysis, DNA
  • Steroids / metabolism
  • Tissue Distribution

Substances

  • Arthropod Proteins
  • Blood Glucose
  • CHH-like protein, shrimp
  • DNA, Complementary
  • Ecdysteroids
  • Invertebrate Hormones
  • Peptides
  • Protein Precursors
  • Steroids

Associated data

  • GENBANK/AF286084
  • GENBANK/AF286092