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Expression of the mouse WNK1 gene in correlation with ganglioside GD3 and functional analysis of the mouse WNK1 promoter

  • Guichao Zeng(corresponding author)
    ,
  • Luoyi Gao
    ,
  • Tian Xia
    ,
  • Yihua Gu
    ,
  • Robert K. Yu
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

WNK1 is one of WNK (With No K=Lysine) protein kinases which comprise a newly described subfamily. Our studies showed that expression of the mouse WNK1 gene was dramatically suppressed in a tumor cell line when its phenotype was altered by suppression of the GD3-synthase gene expression. The mouse WNK1 gene was expressed at a high level at early stage of embryonic brain and its expression decreased as brain developed, similar to the expression pattern of the GD3-synthase gene. To study transcriptional regulation, we cloned a 5′-flanking 1239-bp fragment of the mouse WNK1 gene. This fragment contains a number of potential consensus binding sites for transcription factors, including Sp1, AP2, CCAAT, Est-1, Oct-1, CNBP, and NFkB, but lacks a TATA box. Primer extension identified multiple putative transcriptional initiation sites, including several sites downstream of the ATG codon. Activities of the promoter fragments were assessed in mouse breast Sa/R-MT cells by transient transfection and the results showed that the promoter elements between -700 and -977 is required for maintaining a high level of promoter activity of the TATA-less mouse WNK1 gene.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 233-239 (7 pages)

Journal (Volume, Issue Number)

Gene (Volume 344)

Publication milestones

  • Published - 01/03/2005

Publication status

Published - 01/03/2005

ISSN

0378-1119

Publication IDs

  • Scopus: 12344264912
  • PubMed: 15656989

Publication metrics

Metrics

Scopus
citations
SciVal
citations
10
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1
SciVal
FWCI
0.23
SciVal
Author count
5
SciVal
Paper percentile
61

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Citation count
10
Captures
14

Funding Details

This work was supported in part by NINDS, National Institutes of Health Grant NS11853 and the Combined Intramural Grants Program of Medical College of Georgia.
FundersFunding number
NIH
-
NINDS
R01NS011853