TY - JOUR
T1 - Multiple splicing variants of two new human ATP-binding cassette transporters, ABCC11 and ABCC12
AU - Yabuuchi, Hikaru
AU - Shimizu, Hidetada
AU - Takayanagi, Shin ichiro
AU - Ishikawa, Toshihisa
N1 - Funding Information:
This study was supported by a research grant (H12-Genome-026) entitled “Studies on the genetic polymorphism and function of pharmacokinetics-related proteins in Japanese population” from the Japanese Ministry of Health and Welfare as well as, in part, by research grants of a NEDO project “Development of the hepatocyte-chip for drug toxicity evaluation” and Grant-in-Aid for Creative Scientific Research (No. 13NP0401) of Japan Society for the Promotion of Science.
PY - 2001/11/9
Y1 - 2001/11/9
N2 - Two new human ABC transporters, ABCC11 and ABCC12, were cloned from a cDNA library of human adult liver. ABCC11 and ABCC12 genes consist of 30 and 29 exons, respectively, and they are tandemly located in a tail-to-head orientation on human chromosome 16q12.1. The predicted amino acid sequences of both gene products show a high similarity with ABCC5. The transcripts of ABCC11 and ABCC12 genes were detected by PCR in various adult human tissues, including liver, lung, and kidney, and also in several fetal tissues. By searching cDNA libraries from various human tissues, we have identified alternative splicing variants of ABCC11 and ABCC12 genes at significantly high frequencies. One splice variant lacking the exon 28 corresponded to about 25% of total ABCC11 gene transcripts. Furthermore, four splicing variants encoding putatively short peptides were pre-dominant in ABCC12 gene transcripts. Those splicing variants may represent diverse biological functions of these ABC transporter genes.
AB - Two new human ABC transporters, ABCC11 and ABCC12, were cloned from a cDNA library of human adult liver. ABCC11 and ABCC12 genes consist of 30 and 29 exons, respectively, and they are tandemly located in a tail-to-head orientation on human chromosome 16q12.1. The predicted amino acid sequences of both gene products show a high similarity with ABCC5. The transcripts of ABCC11 and ABCC12 genes were detected by PCR in various adult human tissues, including liver, lung, and kidney, and also in several fetal tissues. By searching cDNA libraries from various human tissues, we have identified alternative splicing variants of ABCC11 and ABCC12 genes at significantly high frequencies. One splice variant lacking the exon 28 corresponded to about 25% of total ABCC11 gene transcripts. Furthermore, four splicing variants encoding putatively short peptides were pre-dominant in ABCC12 gene transcripts. Those splicing variants may represent diverse biological functions of these ABC transporter genes.
KW - ABC transporter
KW - ABCC11
KW - ABCC12
KW - Alternative splicing
KW - Genetic polymorphism
KW - Human chromosome 16
UR - https://www.scopus.com/pages/publications/0035834572
UR - https://www.scopus.com/inward/citedby.url?scp=0035834572&partnerID=8YFLogxK
U2 - 10.1006/bbrc.2001.5865
DO - 10.1006/bbrc.2001.5865
M3 - Article
C2 - 11688999
AN - SCOPUS:0035834572
SN - 0006-291X
VL - 288
SP - 933
EP - 939
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -