Guo, M., Akiyama, Y., House, M.G., Hooker, C.M., Heath, E., Gabrielson, E., Yang, S.C., Han, Y., Baylin, S.B., Herman, J.G. and Brock, M.V. (2004) Hypermethylation of the GATA genes in lung cancer. Clinical Cancer Research, 10, 7917-7924.

has been cited by the following article:

• TITLE: Role of the PEST sequence in the long-type GATA-6 DNA-binding protein expressed in human cancer cell lines

  AUTHORS: Kanako Obayashi, Kayoko Takada, Kazuaki Ohashi, Ayako Kobayashi-Ohashi, Masatomo Maeda

  KEYWORDS: DNA-Binding Protein; GATA-6; Transcription Factor; Leaky Ribosome Scanning; PEST Sequence; Gel Electrophoresis

  JOURNAL NAME: Advances in Bioscience and Biotechnology, Vol.3 No.4, August 23, 2012

  ABSTRACT: GATA-6 mRNA utilizes two Met-codons in frame as translational initiation codons in cultured mammalian cells. Deletion of the nucleotide sequence encoding the PEST sequence between the two initiation codons unusually reduced the protein molecular size on SDS-polyacrylamide gel-electrophoresis. The reduced molecular size is ascribed to the molecular property of GATA-6, since both amino-and carboxy-lterminal tags introduced into GATA-6 were detected on the gel. This PEST sequence seems to contribute to expansion of the long-type GATA-6 molecule. The long-type GATA-6 containing the PEST sequence exhibits more activation potential than that without this sequence, the latter’s activity being similar to that of the short-type GATA-6. We further demonstrated that human colon and lung cancer cell lines express both the long-type GATA-6 and the short-type GATA-6 in their nuclei.