The photoreactivation of 6-4 photoproducts in chloroplast and nuclear DNA depends on the amount of the Arabidopsis UV repair defective 3 protein

被引:0
作者
Zglobicki, Piotr [1 ]
Hermanowicz, Pawel [2 ]
Klodawska, Kinga [3 ]
Bazant, Aneta [1 ]
Labuz, Justyna [2 ]
Grzyb, Joanna [4 ]
Dutka, Malgorzata [5 ]
Kowalska, Ewa [1 ]
Jawor, Joanna [1 ]
Leja, Katarzyna [1 ,6 ]
Banas, Agnieszka Katarzyna [1 ]
机构
[1] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Plant Biotechnol, Gronostajowa 7, PL-30387 Krakow, Poland
[2] Jagiellonian Univ, Malopolska Ctr Biotechnol, Gronostajowa 7A, PL-30387 Krakow, Poland
[3] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Plant Physiol & Biochem, Gronostajowa 7, PL-30387 Krakow, Poland
[4] Univ Wroclaw, Fac Biotechnol, Dept Biophys, F Joliot Curie 14a, PL-50383 Wroclaw, Poland
[5] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Mol Biophys, Gronostajowa 7, PL-30387 Krakow, Poland
[6] Jagiellonian Univ, Doctoral Sch Exact & Nat Sci, Prof S Lojasiewicza 11, PL-30348 Krakow, Poland
来源
BMC PLANT BIOLOGY | 2024年 / 24卷 / 01期
关键词
Arabidopsis; AtUVR3; Chloroplast nucleoid; Photolyase; Photoreactivation; (6-4) pyrimidine-pyrimidone photoproduct; CYCLOBUTANE PYRIMIDINE DIMER; PHOTOLYASE ACTIVITY; MITOCHONDRIAL-DNA; GENE; DAMAGE; GROWTH; RICE; PHOTOREPAIR; EXPRESSION; THALIANA;
D O I
10.1186/s12870-024-05439-0
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background6 - 4 photoproducts are the second most common UV-induced DNA lesions after cyclobutane pyrimidine dimers. In plants, they are mainly repaired by photolyases in a process called photoreactivation. While pyrimidine dimers can be deleterious, leading to mutagenesis or even cell death, 6 - 4 photoproducts can activate specific signaling pathways. Therefore, their removal is particularly important, especially for plants exposed to high UV intensities due to their sessile nature. Although photoreactivation in nuclear DNA is well-known, its role in plant organelles remains unclear. In this paper we analyzed the activity and localization of GFP-tagged AtUVR3, the 6 - 4 photoproduct specific photolyase.ResultsUsing transgenic Arabidopsis with different expression levels of AtUVR3, we confirmed a positive trend between these levels and the rate of 6 - 4 photoproduct removal under blue light. Measurements of 6 - 4 photoproduct levels in chloroplast and nuclear DNA of wild type, photolyase mutants, and transgenic plants overexpressing AtUVR3 showed that the photoreactivation is the main repair pathway responsible for the removal of these lesions in both organelles. The GFP-tagged AtUVR3 was predominantly located in nuclei with a small fraction present in chloroplasts and mitochondria of transgenic Arabidopsis thaliana and Nicotiana tabacum lines. In chloroplasts, this photolyase co-localized with the nucleoid marked by plastid envelope DNA binding protein.ConclusionsPhotolyases are mainly localized in plant nuclei, with only a small fraction present in chloroplasts and mitochondria. Despite this unbalanced distribution, photoreactivation is the primary mechanism responsible for the removal of 6 - 4 photoproducts from nuclear and chloroplast DNA in adult leaves. The amount of the AtUVR3 photolyase is the limiting factor influencing the photoreactivation rate of 6 - 4 photoproducts. The efficient photoreactivation of 6 - 4 photoproducts in 35S: AtUVR3-GFP Arabidopsis and Nicotiana tabacum is a promising starting point to evaluate whether transgenic crops overproducing this photolyase are more tolerant to high UV irradiation and how they respond to other abiotic and biotic stresses under field conditions.
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