The paper uses lentiviral shRNA to deplete each of the three striatin family scaffolds (STRN, SG2NA, zinedin) in primary mouse keratinocytes and fibroblasts, with RNA-seq (3 biological replicates), qPCR validation, western blotting, mass spectrometry, MG132 proteasome inhibition, and wound-healing assays . The knockdown efficiency was markedly better in keratinocytes than fibroblasts (mRNA fold changes of β4.24, β4.18, and β4.35 for STRN, SG2NA, and zinedin in keratinocytes versus β2.67, β2.78, and β3.03 in fibroblasts), which the authors themselves use to explain why keratinocytes showed more robust downstream transcriptional effects.
The central novel observation is that all three knockdowns reduce pYAP(S127) and pYAP(S397) without changing total YAP, and MG132 rescues both pYAP forms β leading the authors to propose striatins protect phosphorylated YAP from proteasomal degradation. However, YAP ubiquitination was not altered, forcing the authors into a ubiquitin-independent degradation hypothesis (c-degrons, lysosomal IKKΞ΅-mediated degradation) that remains speculative. The mass-spectrometry finding that 14-3-3 protein levels drop after STRN/SG2NA depletion offers a partial mechanistic bridge for pYAP(127) loss, but no direct binding data between striatins and pYAP or the proteasome are presented. This is consistent with canonical Hippo logic β LATS-mediated phosphorylation drives YAP degradation and 14-3-3 retention β but here it is inverted: striatin loss appears to increase pYAP turnover without changing upstream LATS/SAV1, an under-explained inconsistency the authors acknowledge.
RNA-seq revealed strikingly non-overlapping transcriptional responses: SG2NA depletion yielded 159 unique DEGs out of 319 in fibroblasts, while zinedin depletion produced 224 unique DEGs in keratinocytes; almost no DEGs were shared between cell types after striatin depletion . Only ENDOU and KRT16 were upregulated across all three keratinocyte knockdowns β both previously unlinked to striatins, and KRT16 ties mechanistically to migration (KRT16 overexpression reduces keratinocyte migration). Wound-healing assays showed migration impairment 3β9 h after wounding for all three KDs, with a minor Ki-67 proliferation reduction (notably zinedin).
The Wnt connection is weak: APCDD1 mRNA rose substantially in RNA-seq (up to 10.1-fold for zinedin) but only 1.5β2.5-fold by qPCR and less than 1.5-fold at the protein level β a classic magnitude discrepancy the authors candidly attribute to sensitivity, normalization, and primary-cell variability. Active Ξ²-catenin changed only modestly. The authors' therapeutic framing (striatins as dual Hippo/Wnt anti-cancer targets) is not supported by the modest, indirect Wnt data presented.
A solid, honest exploratory study whose strongest contribution is the cell-typeβresolved transcriptomic resource and the provocative pYAP-stabilization hypothesis. Confidence in the pYAP mechanism is moderate at best; the migration and KRT16 findings are the most reproducible, directly measured effects. The HippoβSTRIPAK axis itself is well established; what would disconfirm this paper's specific claim is a demonstration that pYAP loss upon striatin depletion persists with simultaneous proteasome and lysosome inhibition, or that re-expression of striatin fails to restore pYAP levels.
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