Isolation and Characterization of a Novel Human Radiosusceptibility Gene, NP95

• Published in: Radiation research 2006-11, Vol.166 (5), p.723-733
• Main Authors: Muto, Masahiro, Fujimori, Akira, Mituru Nenoi, Daino, Kazuhiro, Matsuda, Yoichi, Kuroiwa, Asato, Eiko Kubo, Yasuyoshi Kanari, Makoto Utsuno, Tsuji, Hideo, Ukai, Hideki, Mita, Kazuei, Takahagi, Masahiko, Tatsumi, Kouichi
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; Cell cycle; Cell Line; Cell lines; Complementary DNA; DNA; Dose-Response Relationship, Radiation; Exons; Genes; HEK293 cells; Humans; Kidney - metabolism; Kidney - radiation effects; Mice; Molecular Sequence Data; Polymerase chain reaction; Radiation Dosage; Radiation Tolerance - physiology; Somatic cells; Ubiquitin-Protein Ligases - genetics; Ubiquitin-Protein Ligases - metabolism; Untranslated regions
• ISSN: 0033-7587; 1938-5404
• DOI: 10.1667/RR0459.1

The murine nuclear protein Np95 has been shown to underlie resistance to ionizing radiation and other DNA insults or replication arrests in embryonic stem (ES) cells. Using the databases for expressed sequenced tags and a two-step PCR procedure, we isolated human NP95, the full-length human homologue of the murine Np95 cDNA, which consists of 4,327 bp with a single open reading frame (ORF) encoding a polypeptide of 793 amino acids and 73.3% homology to Np95. The ORF of human NP95 cDNA is identical to the UHRF1 (ubiquitin-like protein containing PHD and RING domain 1). The NP95 gene, assigned to 19p13.3, consists of 18 exons, spanning 60 kb. Several stable transformants from HEK293 and WI38 cells that had been transfected with the antisense NP95 cDNA were, like the murine Np95-knockout ES cells, more sensitive to X rays, UV light and hydroxyurea than the corresponding parental cells. In HEK293 cells, the lack of NP95 did not affect the activities of topoisomerase IIα, whose expression had been demonstrated to be regulated by the inverted CCAAT box binding protein of 90 kDa (ICBP90) that closely resembles NP95 in amino acid sequence and in cDNA but differs greatly in genomic organization. These findings collectively indicate that the human NP95 gene is the functional orthologue of the murine Np95 gene.