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. 2023 Sep 1;37(17-18):861. doi: 10.1101/gad.351178.123

Corrigendum: The Polycomb group proteins bind throughout the INK4A-ARF locus and are disassociated in senescent cells

Adrian P Bracken, Daniela Kleine-Kohlbrecher, Nikolaj Dietrich, Diego Pasini, Gaetano Gargiulo, Chantal Beekman, Kim Theilgaard-Mönch, Saverio Minucci, Bo T Porse, Jean-Christophe Marine, Klaus H Hansen, Kristian Helin
PMCID: PMC10620040  PMID: 37852794

Genes & Development 21: 525–530 (2007)

In the above-mentioned article, we discovered an error in Figure 3A. During the process of compiling the figures, an error occurred wherein a scan of a BMI1 Western blot intended for Figure 4A was erroneously also included in Figure 3A. We presume that the occurrence of a shared BMI1 label and the three-lane configuration in both instances was a contributing factor to this inadvertent error. Subsequent efforts to locate the original experiment proved unsuccessful; however, an alternate replicate of the experiment depicted in Figure 3A was located and is presented below, along with a revised figure legend. This alternate replicate shows that, unlike BMI1, EZH2 protein levels decrease upon serial passaging of mouse embryonic fibroblasts (MEFs). The replicate is in agreement with the original interpretation of the results in Figure 3A, and therefore the error does not impinge on any of the conclusions advanced by Figure 3 or influence any of the findings presented in the manuscript.

Figure 3.

Figure 3.

PcGs and H3K27me3 are lost from the Ink4a-Arf locus in cells undergoing senescence. (A) Western blots of cell lysates prepared from MEFs at increasing passage numbers were probed with the indicated antibodies. (B) qPCR analysis of the indicated genes on mRNA prepared from MEFs at increasing passages. (C) Representation of the mouse Ink4a-Arf gene locus. Amplified regions in D are indicated as red bars. (D) ChIP analysis using the indicated antibodies on the Ink4a-Arf locus in MEFs at increasing passage numbers.

doi:10.1101/gad.351178.123


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