Trends in Cardiovascular Medicine
Volume 19, Issue 6 , Pages 179-182, August 2009

Noncanonical Activity of Seryl-Transfer RNA Synthetase and Vascular Development

  • Atsuo Kawahara

      Affiliations

    • Department of Structural Analysis, National Cardiovascular Center Research Institute, Suita, Osaka, 565-8565, Japan
    • Corresponding Author InformationAddress correspondence to: Atsuo Kawahara, Department of Structural Analysis, National Cardiovascular Center Research Institute, Fujishirodai 5-7-1, Suita, Osaka 565-8565, Japan. Tel.: (+81) 6-6835-5004/2508; fax: (+81) 6-6835-5461. Didier Y. R. Stainier, Department of Biochemistry and Biophysics and the Cardiovascular Research Institute, University of California, San Francisco, 1550 4th St, San Francisco, CA 94158, USA. Tel.: (+1) 415-502-5679; fax: (+1) 415-476-3892.
  • ,
  • Didier Y.R. Stainier

      Affiliations

    • Department of Biochemistry and Biophysics and the Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA
    • Corresponding Author InformationAddress correspondence to: Atsuo Kawahara, Department of Structural Analysis, National Cardiovascular Center Research Institute, Fujishirodai 5-7-1, Suita, Osaka 565-8565, Japan. Tel.: (+81) 6-6835-5004/2508; fax: (+81) 6-6835-5461. Didier Y. R. Stainier, Department of Biochemistry and Biophysics and the Cardiovascular Research Institute, University of California, San Francisco, 1550 4th St, San Francisco, CA 94158, USA. Tel.: (+1) 415-502-5679; fax: (+1) 415-476-3892.

Seryl-transfer RNA synthetase (Sars) is one of the 20 aminoacyl-transfer RNA synthetases that are enzymes essential for protein synthesis; however, the developmental function of Sars has not been elucidated. In zebrafish, impairment of zygotic Sars function leads to a significant dilatation of the aortic arch vessels and aberrant branching of cranial and intersegmental vessels. This abnormal vascular branching in sars mutants can be suppressed by a form of Sars that lacks canonical function, indicating that a noncanonical activity of Sars regulates vascular development. Inhibition or knockdown of vascular endothelial growth factor (Vegf) signaling, which plays pivotal roles in the establishment of the vascular network, suppresses the abnormal vascular branching observed in sars mutants. Here, we discuss the possible functional relationship between Sars function and Vegf signaling.

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PII: S1050-1738(09)00167-4

doi:10.1016/j.tcm.2009.11.001

Trends in Cardiovascular Medicine
Volume 19, Issue 6 , Pages 179-182, August 2009