The new face of the old molecules: crustin Pm4 and transglutaminase type I serving as rnps down-regulate astakine-mediated hematopoiesis

PLoS One. 2013 Aug 27;8(8):e72793. doi: 10.1371/journal.pone.0072793. eCollection 2013.

Abstract

Astakine is an important cytokine that is involved in crustacean hematopoiesis. Interestingly, the protein levels of astakine increased dramatically in plasma of LPS-injected shrimp while mRNA levels remained unchanged. Here, we investigated the involvement of astakine 3'-untranslated region (UTR) in its protein expression. The 3'-UTR of astakine down-regulated the expression of reporter protein but the mRNA stability of reporter gene was unaffected. We identified the functional regulatory elements of astakine 3'-UTR, where 3'-UTR242-483 acted as repressor. The electrophoresis mobility shift assay (EMSA), RNA pull-down assay and LC/MS/MS were performed to identify the protein association. We noted that crustin Pm4 and shrimp transglutaminase I (STG I) were associated to astakine 3'-UTR242-483, while two other proteins have yet to be revealed. Depletion of hemocytic crustin Pm4 and STG I significantly increased the protein level of astakine while astakine mRNA level remained unaffected. Lipopolysaccharide (LPS) stimulated the secretion of crustin Pm4 and STG I from hemocytes to plasma and increased the astakine level to stimulate the hemocytes proliferation. Altogether, we identified the shrimp crustin Pm4 and STG I as novel RNA binding proteins that play an important role in down-regulating astakine expression at post-transcriptional level and are crucial for the maintenance of hematopoiesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / physiology
  • Animals
  • Antimicrobial Cationic Peptides / genetics
  • Antimicrobial Cationic Peptides / metabolism*
  • Arthropod Proteins / genetics
  • Arthropod Proteins / metabolism*
  • Decapoda / genetics
  • Decapoda / metabolism*
  • Down-Regulation / physiology*
  • Hematopoiesis / physiology*
  • Hemocytes / cytology
  • Hemocytes / metabolism
  • RNA Stability / physiology
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / metabolism*
  • Sf9 Cells
  • Spodoptera
  • Transglutaminases / genetics
  • Transglutaminases / metabolism*
  • Vascular Endothelial Growth Factor, Endocrine-Gland-Derived / biosynthesis*
  • Vascular Endothelial Growth Factor, Endocrine-Gland-Derived / genetics

Substances

  • 3' Untranslated Regions
  • Antimicrobial Cationic Peptides
  • Arthropod Proteins
  • Ribonucleoproteins
  • Vascular Endothelial Growth Factor, Endocrine-Gland-Derived
  • Transglutaminases
  • transglutaminase 1

Grants and funding

This study was supported financially by the National Science Council (Grant no. NSC 100-2313-B-002 -041 -MY2) to Yen-Ling Song. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.