Skip NavigationSkip to Content

Cutting Edge: KIR Antisense Transcripts Are Processed into a 28-Base PIWI-Like RNA in Human NK Cells

  1. Author:
    Cichocki, F.
    Lenvik, T.
    Sharma, N.
    Yun, G.
    Anderson, S. K.
    Miller, J. S.
  2. Author Address

    [Cichocki, Frank; Lenvik, Todd; Yun, Gong; Miller, Jeffrey S.] Univ Minnesota, Div Hematol Oncol & Transplantat, Ctr Canc, Minneapolis, MN 55455 USA. [Sharma, Neeraj; Anderson, Stephen K.] NCI, Expt Immunol Lab, Canc & Inflammat Program, Frederick, MD 21702 USA. [Anderson, Stephen K.] NCI, SAIC Frederick Inc, Frederick, MD 21702 USA.;Miller, JS, Univ Minnesota, Div Hematol Oncol & Transplantat, Ctr Canc, MMC 806,Harvard St & E River Rd, Minneapolis, MN 55455 USA.;mille011@umn.edu
    1. Year: 2010
    2. Date: Aug
  1. Journal: Journal of Immunology
    1. 185
    2. 4
    3. Pages: 2009-2012
  2. Type of Article: Article
  3. ISSN: 0022-1767
  1. Abstract:

    Killer Ig-like receptors (KIRs) are expressed in a variegated, clonally restricted fashion on NK cells and are important determinants of NK cell function. Although silencing of individual KIR genes is strongly correlated with the presence of CpG dinucleotide methylation within the promoter, the mechanism responsible for silencing has not been identified. Our results show that antisense transcripts mediate KIR transcriptional silencing through a novel PIWI-like 28-base small RNA. Although PIWI RNA-mediated silencing of transposable elements within germ cells have been described, this is the first report that identifies a PIWI-like RNA in an immune somatic cell lineage and identifies a mechanism that may be broadly used in orchestrating immune development. The Journal of Immunology, 2010, 185: 2009-2012.

    See More

External Sources

  1. DOI: 10.4049/jimmunol.1000855
  2. WOS: 000280661900006

Library Notes

  1. Fiscal Year: FY2009-2010
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