TY - JOUR
T1 - Rice UV-damaged DNA binding protein homologues are most abundant in proliferating tissues
AU - Ishibashi, Toyotaka
AU - Kimura, Seisuke
AU - Yamamoto, Taichi
AU - Furukawa, Tomoyuki
AU - Takata, Kei Ichi
AU - Uchiyama, Yukinobu
AU - Hashimoto, Junji
AU - Sakaguchi, Kengo
PY - 2003/4/10
Y1 - 2003/4/10
N2 - Ultraviolet-damaged DNA binding protein (UV-DDB) is an important factor involved in DNA repair. To study the role of UV-DDB, we attempted to obtain the cDNA and the protein of a plant UV-DDB. We succeeded in isolating both genes for UV-DDB subunits from rice (Oryza sativa cv. Nipponbare), designated as OsUV-DDB1 and OsUV-DDB2. OsUV-DDB2 (65 kDa) was much larger than human UV-DDB2, but immunoprecipitation and gel mobility shift assay suggested that OsUV-DDB2 is a plant counterpart of UV-DDB2. The transcripts were expressed in proliferating tissues such as the meristem, but were detected at only low levels in the mature leaves, although the leaves are strongly exposed to UV. These transcripts were induced in the meristem after UV-irradiation. The expression levels of OsUV-DDB were significantly reduced when cell proliferation was temporarily halted. These results indicated that the level of OsUV-DDB expression is correlated with cell proliferation, and its expression may be required mostly for DNA repair in DNA replication.
AB - Ultraviolet-damaged DNA binding protein (UV-DDB) is an important factor involved in DNA repair. To study the role of UV-DDB, we attempted to obtain the cDNA and the protein of a plant UV-DDB. We succeeded in isolating both genes for UV-DDB subunits from rice (Oryza sativa cv. Nipponbare), designated as OsUV-DDB1 and OsUV-DDB2. OsUV-DDB2 (65 kDa) was much larger than human UV-DDB2, but immunoprecipitation and gel mobility shift assay suggested that OsUV-DDB2 is a plant counterpart of UV-DDB2. The transcripts were expressed in proliferating tissues such as the meristem, but were detected at only low levels in the mature leaves, although the leaves are strongly exposed to UV. These transcripts were induced in the meristem after UV-irradiation. The expression levels of OsUV-DDB were significantly reduced when cell proliferation was temporarily halted. These results indicated that the level of OsUV-DDB expression is correlated with cell proliferation, and its expression may be required mostly for DNA repair in DNA replication.
KW - Oryza sativa L. cv. Nipponbare
KW - Plant UV repair
KW - UV-damaged DNA binding protein
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000182939500008
UR - https://openalex.org/W2012776632
UR - https://www.scopus.com/pages/publications/0038242512
U2 - 10.1016/S0378-1119(03)00447-5
DO - 10.1016/S0378-1119(03)00447-5
M3 - Journal Article
C2 - 12711392
SN - 0378-1119
VL - 308
SP - 79
EP - 87
JO - Gene
JF - Gene
IS - 1-2
ER -