Literature DB >> 11997107

Identification and characterization of an isoform of murine Mpl.

Diana F Sabath1, Cathy Lofton-Day, Nancy Lin, Si Lok, Kenneth Kaushansky, Virginia C Broudy.   

Abstract

A new isoform of the full-length murine thrombopoietin (Tpo) receptor was isolated from a murine spleen cDNA library. This isoform, c-mpl-II, differs from full-length c-mpl (c-mpl-I) by virtue of deletion of 180 nucleotides that encode 60 amino acids located in the extracellular domain of Mpl. Normal murine megakaryocytes were found to express both c-mpl-I and c-mpl-II transcripts. BaF3 cells transfected with c-mpl-I expressed a 95 kDa protein that was displayed on the cell surface and bound 125I-Tpo. BaF3 cells transfected with c-mpl-II expressed a 70 kDa protein. However, these cells were not able to bind 125I-Tpo and surface display of Mpl-II could not be detected. In summary, c-mpl-II is an isoform of murine Mpl expressed by megakaryocytes that lacks a 60 amino acid region required for surface expression of the protein.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11997107     DOI: 10.1016/s0167-4781(01)00357-8

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  1 in total

1.  Identification of the residues in the extracellular domain of thrombopoietin receptor involved in the binding of thrombopoietin and a nuclear distribution protein (human NUDC).

Authors:  Wei-Min Chen; Bo Yu; Qing Zhang; Peilin Xu
Journal:  J Biol Chem       Date:  2010-06-07       Impact factor: 5.157

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.