Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P56851 (
epididymal
)
11,273
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
We report the cloning and expressional analysis of rat
brain endothelial cell derived gene-1
(
BEC-1
), detected as a gene dominantly expressed in rat brain endothelial cells by the use of suppression subtractive hybridization technique. The complementary deoxyribonucleic acid sequence of
BEC-1
messenger ribonucleic acid was completely determined with a full length of 3410 bp. The open reading frame within the sequence consisted of 522 bp, and the predicted protein sequence was 173 amino acid residues.
BEC-1
gene was thought to be rat
tumor suppressor candidate 5
(
TUSC5
), since
BEC-1
had considerable homology with both mouse
TUSC5
and human located at 17-p-13 point three 1 (LOST1) categorized as human
TUSC5
(identities of 97% and 85%, respectively), which were recently identified as a novel tumor suppressor gene candidate. Expressional analyses for
BEC-1
mRNA with real-time PCR and of
BEC-1
protein by Western blotting demonstrated that both were dominantly expressed in the adipose tissues of Sprague-Dawley (SD) rats. We analyzed and compared the differential expressions of
BEC-1
(
TUSC5
) mRNA and protein in fat tissues between obese homozygous (fa/fa) and lean wild-type (+/+) Zucker rats. Both expressions in the
epididymal
white adipose tissue (WAT) were highest, followed by those in the interscapular brown adipose tissue (BAT), subcutaneous, and mesenteric WATs, respectively. Interestingly, both expressions in
epididymal
WAT of obese Zucker rats were significantly lower than those in lean rats. Although cold exposure at 4 degrees C for 6 h significantly stimulated uncoupling protein-1 (UCP-1) mRNA expression, it significantly inhibited
BEC-1
(
TUSC5
) mRNA expression in the interscapular BAT. These data indicated that rat
BEC-1
(
TUSC5
) was abundantly expressed in adipose tissues, and that it might be involved in their regulation independently of UCP-1.
...
PMID:Molecular cloning and characterization of rat brain endothelial cell derived gene-1 (tumor suppressor candidate 5) expressing abundantly in adipose tissues. 1700 98