Skip NavigationSkip to Content

Evi27 encodes a novel membrane protein with homology to the IL17 receptor

  1. Author:
    Tian, E. M.
    Sawyer, J. R.
    Largaespada, D. A.
    Jenkins, N. A.
    Copeland, N. G.
    Shaughnessy, J. D.
  2. Author Address

    Shaughnessy JD Univ Arkansas Med Sci, Arkansas Canc Res Ctr Little Rock, AR 72205 USA Univ Arkansas Med Sci, Arkansas Canc Res Ctr Little Rock, AR 72205 USA Univ Minnesota, Dept Genet Cell Biol & Dev, Ctr Canc Minneapolis, MN 55455 USA NCI, Frederick Canc Res & Dev Ctr, Mouse Canc Genet Program Frederick, MD 21702 USA
    1. Year: 2000
  1. Journal: Oncogene
    1. 19
    2. 17
    3. Pages: 2098-2109
  2. Type of Article: Article
  1. Abstract:

    Evi27 is a common site of retroviral integration in BXH2 murine myeloid leukemias. Here me show that integration at Evi27 occurs in a CpG island similar to 6 kb upstream from a novel gene (designated Evi27) with homology to the IL17 receptor (Il17r) and that proviral integrations result in increased expression of the Evi27 protein on the cell surface. The human EVI27 homology was also cloned and mapped to chromosome 3p21, Multiple Evi27 isoforms were detected at the RNA and protein level in both human and mouse, indicating that Evi27 expression is complex. Some of the isoforms are shown to likely represent secreted soluble forms of the protein produced by intron incorporation or by proteolytic cleavage. In the mouse, highest Evi27 expression occurs in liver and testes with lower expression in kidney and lung, In humans, EVI27 is expressed at high levels in the kidney, with moderate levels in the liver, brain, and testes. Within hematopoietic cells, Evi27 expression is restricted. Northern and Western analysis showed that Evi27 is expressed in selected T-cell B-cell and myeloid cell lines. These results suggest that Evi27 expression is tightly regulated during hematopoietic differentiation. Collectively, these studies identify a nea member of the cytokine receptor family whose increased and uncoordinated expression may lead to myeloid leukemia by altering Evi27's normal ability to control the growth and/or differentiation of hematopoietic cells. [References: 45]

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel