TY - JOUR
T1 - Isolation of cDNA for a novel human protein KNP-I that is homologous to the E. coli SCRP-27A protein from the autoimmune polyglandular disease type I (APECED) region of chromosome 21q22.3
AU - Nagamine, Kentaro
AU - Kudoh, Jun
AU - Minoshima, Shinsei
AU - Kawasaki, Kazuhiko
AU - Asakawa, Shuichi
AU - Ito, Fumiaki
AU - Shimizu, Nobuyoshi
N1 - Funding Information:
The authors thank Drs. H. Ichikawa and M. Ohki (National Cancer Center Research Institute, Tokyo, Japan) for the NotI linking clones, Dr. E. Bakker (Leiden University, Leiden, Netherlands) for the D21S25 marker (10.2), and Drs. J. Hazan and J. Weissenbach (Genethon, Evry, France) for the D21S154 marker (IP21K443). This work was supported in part by Grants in Aid for Creative Basic Research (Human Genome Program), Scientific Research on Priority Areas, and Scientific Research from the Ministry of Education, Science and Culture of Japan; the Special Coordination Funds for Promoting Science and Technology from the Science and Technology Agency (STA) of Japan; and Fund for Human Genome Sequencing Project from the Japan Information Center of Science and Technology (JICST).
PY - 1996/8/14
Y1 - 1996/8/14
N2 - We have isolated cDNA clones for a novel human protein KNP-I from fetal brain and bone marrow cDNA libraries. Northern blot analysis indicated that the KNP-I gene is ubiquitously expressed in various human tissues. Significant homology of the KNP-I protein with Escherichia coli anti-sigma cross-reacting protein (SCRP-27A) (44% identity) and zebrafish (Brachydanio rerio) es1 protein (49% identity) suggested that the KNP-I protein may be involved in a basic cellular function. Genomic sequencing revealed that the KNP-I gene consists of seven exons spanning 12 kb. Exon 5 was involved in alternative splicing. The KNP-I gene was mapped between D21S1460 and D21S25 on human chromosome 21q22.3, 26 kb distal to a Not I site of D21S1460. Thus, this novel KNP-I gene could be a candidate gene for autoimmune polyglandular disease type I (APECED) and other disorders mapped to this region.
AB - We have isolated cDNA clones for a novel human protein KNP-I from fetal brain and bone marrow cDNA libraries. Northern blot analysis indicated that the KNP-I gene is ubiquitously expressed in various human tissues. Significant homology of the KNP-I protein with Escherichia coli anti-sigma cross-reacting protein (SCRP-27A) (44% identity) and zebrafish (Brachydanio rerio) es1 protein (49% identity) suggested that the KNP-I protein may be involved in a basic cellular function. Genomic sequencing revealed that the KNP-I gene consists of seven exons spanning 12 kb. Exon 5 was involved in alternative splicing. The KNP-I gene was mapped between D21S1460 and D21S25 on human chromosome 21q22.3, 26 kb distal to a Not I site of D21S1460. Thus, this novel KNP-I gene could be a candidate gene for autoimmune polyglandular disease type I (APECED) and other disorders mapped to this region.
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U2 - 10.1006/bbrc.1996.1218
DO - 10.1006/bbrc.1996.1218
M3 - Article
C2 - 8753807
AN - SCOPUS:0030583302
SN - 0006-291X
VL - 225
SP - 608
EP - 616
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -