Skip NavigationSkip to Content

Molecular Cloning of Fkhrl1p2, a Member of the Developmentally Regulated Fork Head Domain Transcription Factor Family

  1. Author:
    Dasilva, L.
    Kirken, R. A.
    Taub, D. D.
    Evans, G. A.
    Duhe, R. J.
    Bailey, M. A.
    Farrar, W. L.
  2. Author Address

    Dasilva L SAIC FREDERICK IRSP DIV BASIC SCI FREDERICK, MD 21702 USA NIA IMMUNOL LAB GRC NIH BALTIMORE, MD 21224 USA NCI FREDERICK CANC RES & DEV CTR MOL IMMUNOREGULAT LAB CYTOKINE MOL MECH SECT FREDERICK, MD 21702 USA
    1. Year: 1998
  1. Journal: Gene
    1. 221
    2. 1
    3. Pages: 135-142
  2. Type of Article: Article
  1. Abstract:

    Here we report the expression of a fork head domain protein in human T helper cells. We cloned and characterized a fork head cDNA from human T helper cell mRNA using differential display RT-PCR. The cDNA contains a 546-nucleotide (nt) open reading frame (ORF) that codes for the carboxyl-terminal 180 amino acids (aa) of the recently identified fkhrl1 gene. This ORF does not contain the characteristic DNA-binding domain found in members of the forkhead protein family. In-vitro transcription/translation of this cDNA expressed a protein of approximately 20 kDa. We have generated antibodies that specifically immunoprecipitated the in-vitro-translated 20-kDa protein. This antibody also recognizes in human T lymphocytes a 70-kDa protein corresponding in size to that predicted for the fkhrl1 gene product. The mRNA levels for fkhrl1 is elevated in T helper-induced lymphocytes in comparison to PHA-stimulated T lymphocytes. Further characterization of FKHRL1 and its related family members should shed light on the transcriptional mechanisms of this fork head gene subfamily and their role in T helper cell differentiation and regulation of cell growth. (C) 1998 Elsevier Science B.V. All rights reserved. [References: 26]

    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