Introduction
a member of the POU domain factors, is involved
in the regulation of expression of many tissue-specific and
house-keeping genes by recruiting specialized coactivators of
transcription.
PMID: 14729276,
PMID: 11683265,
PMID: 11380252
Normal Expression
Oct-1Z is another ubiquitously expressed Oct-1
isoform, its transcript being detected in all mouse tissues
examined, including the mammary gland, liver, lung, kidney, spleen,
small intestine mucosa, uterus, and ovary.
PMID: 14729276
the POU-domain of Oct-1 has been highly conserved
during vertebrate evolution and that Oct-1 mRNA is widely expressed
in various organs of adult rat.
PMID: 8424955
Abnormal Expression
OCT-1 is expressed in chronic gastritis,
particularly when it is adjacent to IM and is expressed in 87% of IM
foci. Furthermore, 74% of the gastric carcinomas were positive for
OCT-1 and a strong association was observed between OCT-1 expression
and intestinal-type carcinoma.
PMID: 16278805
Function
tissue-specific expression of Oct-1L and Oct-1R
in lymphocytes and their structural differences from the
ubiquitously expressed Oct-1 isoforms may be related to B and T cell
differentiation and/or expression of the immunoglobulin genes.
PMID: 11683265
Oct-1 acts as a transcriptional repressor of
promoters of genes expressed in endothelial cells.
PMID: 9694713
Applications
Gel Shift Assay (Gel)
we evaluated OCT-1 binding by electrophoretic mobility shift assay and activation of the CDX2 promoter by co-transfecting a CDX2 promoter/reporter construct with an OCT-1 expression vector in two gastric carcinoma cell lines, GP220 and MKN45. PMID: 16278805
Immunohistochemistry (IHC)
OCT-1 protein expression was evaluated by
immunohistochemistry in 31 biopsies with chronic gastritis, 15
biopsies with foci of IM and adjacent gastric mucosa and 42 gastric
carcinomas.
PMID: 16278805
By using the tissue microarray technique, we have
performed an immunohistochemical study of OCT.1, OCT.2 and BOB.1 in
325 classical Hodgkin's lymphoma cases.
PMID: 15257313
Immunohistochemical examination of rheumatoid
arthritis (RA) synovial tissue revealed simultaneous expression of
various transcription factors (NF-kappa B, c-Jun (a component of
AP-1), cAMP responsive element binding protein (CREB), and OCT-1).
The early passage RA synovial cells were treated with interleukin 1
beta (IL1 beta) and confirmed translocation of transcription factors
into the nucleus by western blotting, and their DNA binding activity
by gel shift assays.
PMID: 9797555
Immunoprecipitation (IP)
nucleoprotein extracts showing decreased
DNA-binding activity had normal amounts of Oct-1 proteins as
determined by immunoprecipitation, implying a functional defect in
the Oct-1 protein.
PMID: 8814238