ECSIT Is a Critical Factor for Controlling Intestinal Homeostasis and Tumorigenesis through Regulating the Translation of YAP Protein

Abstract: The intestinal epithelium is the fastest renewing tissue in mammals and its regenerative process must be tightly controlled to minimize the risk of dysfunction and tumorigenesis. The orderly expression and activation of Yes‐associated protein (YAP) are the key steps in driving intestinal regeneration and crucial for intestinal homeostasis. However, the regulatory mechanisms controlling this process remain largely unknown. Here, it is discovered that evolutionarily conserved signaling intermediate in Toll pathways (ECSIT), a multi‐functional protein, is enriched along the crypt–villus axis. Intestinal cell‐specific ablation of ECSIT results in the dysregulation of intestinal differentiation unexpectedly accompanied with enhanced YAP protein dependent on translation, thus transforming intestinal cells to early proliferative stem “‐like” cells and augmenting intestinal tumorigenesis. Loss of ECSIT leads to metabolic reprogramming in favor of amino acid–based metabolism, which results in demethylation of genes encoding the eukaryotic initiation factor 4F pathway and their increased expression that further promotes YAP translation initiation culminating in intestinal homeostasis imbalance and tumorigenesis. It is also shown that the expression of ECSIT is positively correlated with the survival of patients with colorectal cancer. Together, these results demonstrate the important role of ECSIT in regulating YAP protein translation to control intestinal homeostasis and tumorigenesis.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
ECSIT Is a Critical Factor for Controlling Intestinal Homeostasis and Tumorigenesis through Regulating the Translation of YAP Protein ; day:06 ; month:07 ; year:2023 ; extent:17
Advanced science ; (06.07.2023) (gesamt 17)

Creator
Jiang, Yuying
Ma, Chunmei
Hu, Yingchao
Yang, Yongbing
Ma, Chanyuan
Wu, Chunyan
Liu, Lu
Wen, Shuang
Moynagh, Paul N.
Wang, Bingwei
Yang, Shuo

DOI
10.1002/advs.202205180
URN
urn:nbn:de:101:1-2023070615284966139287
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:59 AM CEST

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Associated

  • Jiang, Yuying
  • Ma, Chunmei
  • Hu, Yingchao
  • Yang, Yongbing
  • Ma, Chanyuan
  • Wu, Chunyan
  • Liu, Lu
  • Wen, Shuang
  • Moynagh, Paul N.
  • Wang, Bingwei
  • Yang, Shuo

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