Transmembrane protein 150b attenuates BMP signaling in the Xenopus organizer

J Cell Physiol. 2023 Aug;238(8):1850-1866. doi: 10.1002/jcp.31059. Epub 2023 Jul 12.

Abstract

The vertebrate organizer is a specified embryonic tissue that regulates dorsoventral patterning and axis formation. Although numerous cellular signaling pathways have been identified as regulators of the organizer's dynamic functions, the process remains incompletely understood, and as-yet unknown pathways remain to be explored for sophisticated mechanistic understanding of the vertebrate organizer. To identify new potential key factors of the organizer, we performed complementary DNA (cDNA) microarray screening using organizer-mimicking Xenopus laevis tissue. This analysis yielded a list of prospective organizer genes, and we determined the role of six-transmembrane domain containing transmembrane protein 150b (Tmem150b) in organizer function. Tmem150b was expressed in the organizer region and induced by Activin/Nodal signaling. In X. laevis, Tmem150b knockdown resulted in head defects and a shortened body axis. Moreover, Tmem150b negatively regulated bone morphogenetic protein (BMP) signaling, likely via physical interaction with activin receptor-like kinase 2 (ALK2). These findings demonstrated that Tmem150b functions as a novel membrane regulatory factor of BMP signaling with antagonistic effects, contributing to the understanding of regulatory molecular mechanisms of organizer axis function. Investigation of additional candidate genes identified in the cDNA microarray analysis could further delineate the genetic networks of the organizer during vertebrate embryogenesis.

Keywords: Spemann organizer; Xenopus; bone morphogenetic proteins; embryogenesis; transmembrane protein 150B.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Patterning / genetics
  • DNA, Complementary / metabolism
  • Gene Expression Regulation, Developmental / genetics
  • Prospective Studies
  • Signal Transduction*
  • Xenopus Proteins* / genetics
  • Xenopus Proteins* / metabolism
  • Xenopus laevis / genetics
  • Xenopus laevis / metabolism

Substances

  • Xenopus Proteins
  • DNA, Complementary