Expression and functional characterization of Xhmg-at-hook genes in Xenopus laevis

PLoS One. 2013 Jul 25;8(7):e69866. doi: 10.1371/journal.pone.0069866. Print 2013.

Abstract

High Mobility Group A proteins (HMGA1 and HMGA2) are architectural nuclear factors involved in development, cell differentiation, and cancer formation and progression. Here we report the cloning, developmental expression and functional analysis of a new multi-AT-hook factor in Xenopus laevis (XHMG-AT-hook) that exists in three different isoforms. Xhmg-at-hook1 and 3 isoforms, but not isoform 2, are expressed throughout the entire development of Xenopus, both in the maternal and zygotic phase. Localized transcripts are present in the animal pole in the early maternal phase; during the zygotic phase, mRNA can be detected in the developing central nervous system (CNS), including the eye, and in the neural crest. We show evidence that XHMG-AT-hook proteins differ from typical HMGA proteins in terms of their properties in DNA binding and in protein/protein interaction. Finally, we provide evidence that they are involved in early CNS development and in neural crest differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Differentiation
  • Central Nervous System / cytology
  • Central Nervous System / growth & development
  • Central Nervous System / metabolism
  • Embryo, Nonmammalian
  • Eye / cytology
  • Eye / growth & development
  • Eye / metabolism
  • Gene Expression Regulation, Developmental
  • High Mobility Group Proteins / genetics*
  • High Mobility Group Proteins / metabolism
  • Molecular Sequence Data
  • Morphogenesis / genetics*
  • Neural Crest / cytology
  • Neural Crest / growth & development
  • Neural Crest / metabolism
  • Protein Binding
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Xenopus laevis / genetics*
  • Xenopus laevis / growth & development
  • Xenopus laevis / metabolism
  • Zygote / cytology
  • Zygote / growth & development
  • Zygote / metabolism

Substances

  • High Mobility Group Proteins
  • RNA, Messenger

Grants and funding

This work was supported by PRIN (Research Programmes of National Interest) 2007–2009 contribution to G.M. and to R.V., Università degli Studi di Trieste, project “Rete Nazionale Proteomica” FIRB (Fund for investment in basic research) 2008-RBRN07BMCT to G.M. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.