Cloning and characterization of sarco/endoplasmic reticulum Ca2+-ATPase (SERCA) from crayfish axial muscle

Z. Zhang, D. Chen, M. G. Wheatly

Research output: Contribution to journalArticlepeer-review

34 Scopus citations


The discontinuous pattern of muscle growth during the moulting cycle of a freshwater crustacean (the crayfish Procambarus clarkii) was used as a model system to examine the regulation of the expression of Sarco/Endoplasmic Reticulum Ca2+-ATPase (SERCA). We describe the cloning, sequencing and characterization of a novel SERCA cDNA (3856 bp) obtained from crayfish axial abdominal muscle by reverse transcription/polymerase chain reaction (RT-PCR) followed by rapid amplification of cDNA ends (RACE). This complete sequence contains a 145 base pair (bp) noncoding region at the 5′ end, a 3006 bp open reading frame coding for 1002 amino acid residues with a molecular mass of 110kDa and 705bp of untranslated region at the 3′ end. This enzyme contains all the conserved domains found in 'P'-type ATPases, and the hydropathy profile suggests a transmembrane organization typical of other SERCAs. It exhibits 80 % amino acid identity with Drosophila melanogaster SERCA, 79 % identity with Artemia franciscana SERCA, 72 % identity with rabbit fast-twitch muscle neonatal isoform SERCA1b, 71 % identity with slow-twitch muscle isoform SERCA2 and 67 % identity with SERCA3. Sequence alignment revealed that regions anchoring the cytoplasmic domain in the membrane were highly conserved and that most differences were in the NH2 terminus, the central loop region and the COOH terminus. Northern analysis of total RNA from crayfish tissues probed with the 460 bp fragment initially isolated showed four bands (7.6, 7.0, 5.8 and 4.5 kilobases) displaying tissue-specific expression. SERCA was most abundant in muscle (axial abdominal, cardiac and stomach), where it is involved in Ca2+ resequestration during relaxation, and in eggs, where it may be implicated in early embryogenesis. The level of SERCA mRNA expression in axial abdominal muscle varied during the moulting cycle as determined by slot-blot analysis. SERCA expression was greatest during intermoult and decreased to approximately 50 % of this level during pre- and postmoult. Patterns of gene expression for SERCA and other sarcomeric proteins during the crustacean moulting cycle may be regulated by ecdysteroids and/or mechanical stimulation.

Original languageEnglish (US)
Pages (from-to)3411-3423
Number of pages13
JournalJournal of Experimental Biology
Issue number22
StatePublished - 2000
Externally publishedYes


  • Crustacea
  • Moulting cycle
  • Muscle
  • Procambarus clarkii
  • Sarco/endoplasraic reticulum Ca-ATPase
  • Tissue-specific distribution
  • cDNA sequence
  • mRNA expression

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics
  • Physiology
  • Aquatic Science
  • Animal Science and Zoology
  • Molecular Biology
  • Insect Science


Dive into the research topics of 'Cloning and characterization of sarco/endoplasmic reticulum Ca2+-ATPase (SERCA) from crayfish axial muscle'. Together they form a unique fingerprint.

Cite this