Editorial Note: Global Regulator SATB1 Recruits β-Catenin and Regulates TH2 Differentiation in Wnt-Dependent Manner

Abstract
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TopicsWnt/β-catenin signaling in development and cancer · Cancer Cells and Metastasis · Connective Tissue Growth Factor Research
Following the publication of the Expression of Concern on this article [1,2], concerns were raised about regions of similarity within the first two lanes in the left panel of Fig S2A of [1], and that [1] states that “thymocyte viability was not significantly reduced even without using the OP9-DL1 co-culture system (Figure S5A)” without viability percentages or statistical test results in the text or figure legend.
As noted in [2], the images provided in S1 File in [2] to support the left western blot panel of Figure S2A in [1] do not appear to match the published figure panel and did not clarify the concerns about discontinuities or similarities in the published figure. The published figure has a stronger and clearer interaction signal than the underlying images; however, the underlying images – while different from the published figure – show a band in the position that would indicate an interaction, and support the conclusion.
The corresponding author responded to state the following:
The PLOS Biology Editors issue this Editorial Note to provide an update to the Expression of Concern [2] previously issued on this article [1] and to provide readers with the additional information provided about Figure S5.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Notani D, Gottimukkala KP, Jayani RS, Limaye AS, Damle MV, Mehta S, et al. Global regulator SATB 1 recruits beta-catenin and regulates T(H)2 differentiation in Wnt-dependent manner. P Lo S Biol. 2010;8(1):e 1000296. doi: 10.1371/journal.pbio.1000296 20126258 PMC 2811152 · doi ↗ · pubmed ↗
- 2PLOS Biology Editors. Expression of Concern: Global Regulator SATB 1 Recruits β-Catenin and Regulates TH 2 Differentiation in Wnt-Dependent Manner. P Lo S Biol. 2022;20(11):e 3001908. doi: 10.1371/journal.pbio.3001908 36417696 PMC 9683845 · doi ↗ · pubmed ↗
