Comment on “Increased MKK4 Abundance with Replicative Senescence Is Linked to the Joint Reduction of Multiple MicroRNAs”

Sci. Signal., 20 July 2010
Vol. 3, Issue 131, p. lc1
DOI: 10.1126/scisignal.3131lc1

Comment on “Increased MKK4 Abundance with Replicative Senescence Is Linked to the Joint Reduction of Multiple MicroRNAs”

  1. Ugo Moens*,
  2. Alexey Shiryaev, and
  3. Gianina Dumitriu
  1. Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, N-9037 Tromsø, Norway.
  1. *Corresponding author. E-mail, ugo.moens{at}uit.no; telephone, +47-77644622; fax, +47-77645350

Abstract

Marasa et al. (Research Article, 27 October 2009, DOI: 10.1126/scisignal.2000442) reported that the human kinase p38–regulated/activated protein kinase (PRAK) was phosphorylated on residue Ser93 in senescent cells. We have been unable to detect phosphorylation at this site with the antibody that they used, and the commercial supplier of this antibody has discontinued its availability, which casts doubt on whether this residue of PRAK is phosphorylated.

Citation:

U. Moens, A. Shiryaev, and G. Dumitriu, Comment on “Increased MKK4 Abundance with Replicative Senescence Is Linked to the Joint Reduction of Multiple MicroRNAs”. Sci. Signal. 3, lc1 (2010).
Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882