Figures
Fig 5 is incorrect. The authors have provided the correct Fig 5 here.
(A) In the left panel, over-night cultures of single mutants ΔcshA, ΔY and YΔ2–24 and double mutants ΔYΔcshA and YΔ2–24ΔcshA were diluted, spotted on agar-plates, and incubated at the indicated temperatures and times. In the right panel, over-night cultures were spotted on horse-blood-agar. (B) Transformants of strain ΔYΔcshA with plasmids expressing variants of RNase Y were selected at 42°C, then restreaked and grown over night at 42°C. Finally the cultures were diluted and spotted at the indicated temperatures. ΔYΔcshA with pYΔ2–24 grows significantly better than the other strains at 24°C. (C) Cartoon showing the four versions of RNase Y expressed from the plasmids; wild-type RNase Y (pY), anchorless RNase Y (pYΔ2–24), RNase Y active site mutant (pY367AA), and anchorless RNase Y active site mutant (pYΔ2–24,367AA). (D) The YΔ2–24ΔcshA strain was transformed with the plasmids expressing the wild-type RNase Y, Y367AA or YΔ2–24,367AA. Overnight cultures were diluted, spotted on agar-plates and incubated at the indicated temperatures for the indicated period of time. Both pY and pY367AA inhibit growth at 24°C. (E) Cartoon showing how the wild-type RNase Y and Y367AA can anchor the YΔ2–24 protein back to the membrane, via dimer-formation.
Reference
Citation: Khemici V, Prados J, Linder P, Redder P (2016) Correction: Decay-Initiating Endoribonucleolytic Cleavage by RNase Y Is Kept under Tight Control via Sequence Preference and Sub-cellular Localisation. PLoS Genet 12(9): e1006320. https://doi.org/10.1371/journal.pgen.1006320
Published: September 14, 2016
Copyright: © 2016 Khemici et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.