Skip NavigationSkip to Content

Isolation and preliminary characterization of the human and mouse homologues of the bacterial cell cycle gene era

  1. Author:
    Britton, R. A.
    Chen, S. M.
    Wallis, D.
    Koeuth, T.
    Powell, B. S.
    Shaffer, L. G.
    Largaespada, D.
    Jenkins, N. A.
    Copeland, N. G.
    Court, D. L.
    Lupski, J. R.
  2. Author Address

    Lupski JR Baylor Coll Med, Dept Mol & Human Genet Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet Houston, TX 77030 USA Baylor Coll Med, Dept Pediat Houston, TX 77030 USA NCI, Frederick Canc Res & Dev Ctr, DBS, Moust Canc Genet Program Frederick, MD 21702 USA
    1. Year: 2000
  1. Journal: Genomics
    1. 67
    2. 1
    3. Pages: 78-82
  2. Type of Article: Article
  1. Abstract:

    Era is an essential GTPase that is required for proper cell cycle progression and cell division in Escherichia coli and is found in nearly all bacteria sequenced to date. To determine whether Era is also present in eukaryotic organisms, we searched the dbEST database and found EST clones coding for proteins that were similar to Era. Full sequencing of these ESTs from human and mouse identified a conserved homologue, ERAL1 (Era-like I). ERAL1 maps to 17q11.2 in human and is located in the syntenic region of mouse chromosome II. ERAL1 may be an attractive candidate for a tumor suppressor gene since ERAL1 is located in a chromosomal region Ts here loss of heterozygosity is often associated with various types of cancer. (C) 2000 Academic Press. [References: 29]

    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