Molecular and Cellular Biology, April 2006, p. 3337, Vol. 26, No. 8
0270-7306/06/$08.00+0 doi:10.1128/MCB.26.8.3337.2006
| AUTHOR'S CORRECTION |
Sinsheimer Laboratories, Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Cruz, California 95064, and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California 94143-0450
Volume 23, no. 17, p. 6327-6337, 2003. We have been unable to reproduce a control experiment reported in this paper. Specifically, we found that 25 µM 1-naphthol-methyl PP1 (1NM-PP1) causes a G1 delay in wild-type cells that is similar to the delay observed in elm1-as cells. While attempting to reproduce this control, we found that addition of supplemental adenine to yeast extract-peptone-dextrose (YPD) growth medium significantly reduces the effects of 1NM-PP1 on wild-type cells. Since our strains are ade and grow slowly on YPD medium, we often supplement the media with additional adenine. The addition of adenine to 100 mg/liter largely eliminates the G1 delay observed in wild-type cells in the presence of 25 µM 1NM-PP1. We also found that the defects in septin organization that we observed before bud emergence were seen only at high concentrations of 1NM-PP1 (25 µM). They may therefore be the combined result of full inhibition of elm1-as and partial inhibition of other kinases. Alternatively, high concentrations of 1NM-PP1 may be necessary to achieve full inhibition of elm1-as. The other results of the paper are unaffected.
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