The C-terminal region of Schizosaccaromyces pombe proliferating cell nuclear antigen is essential for DNA polymerase activity

被引:17
|
作者
Kelman, Z
Zuo, SJ
Arroyo, MP
Wang, TSF
Hurwitz, J
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Mol Biol, New York, NY 10021 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
关键词
D O I
10.1073/pnas.96.17.9515
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proliferating cell nuclear antigen (PCNA), the processivity factor (sliding clamp) of DNA polymerases (Pols), plays essential roles in DNA metabolism, In this report, we examined the functional role of the C-terminal region of Schizosaccaromyces pombe PCNA both in vitro and in vivo. The deletion or Ala substitution of the last 9 aa (252-260A), as well as Ala replacement of only 4 aa (252-255A) at the C terminus, failed to substitute for the wild-type PCNA protein for cell growth in S, pombe, Two other PCNA mutant proteins, A251V and K253E, exhibited cold-sensitive phenotypes. Several yeast strains harboring mutations, including those at the acidic C-terminal region, showed elevated sensitivity to DNA damage. The ability of the mutant PCNA proteins to stimulate DNA synthesis by Pol delta and Pol epsilon also was studied in vitro, The mutant proteins that did not support cell growth and a mutant protein containing a single amino acid substitution at position 252, where Pro is replaced by Ala, stimulated Pol delta and Pol epsilon activities poorly, All mutant PCNA proteins, however, were assembled around DNA by the clamp loader, replication factor C, efficiently. Thus, the C-terminal region of PCNA is important for interactions with both Pol delta and Pol epsilon and for cell survival after DNA damage. The C terminus of sliding clamps from other organisms has been shown to be important for clamp loading as well as polymerase interactions. The relationship between the conserved sequence in this region in different organisms is discussed.
引用
收藏
页码:9515 / 9520
页数:6
相关论文
共 50 条
  • [41] MECHANISM OF ELONGATION OF PRIMED DNA BY DNA POLYMERASE-DELTA, PROLIFERATING CELL NUCLEAR ANTIGEN, AND ACTIVATOR-1
    LEE, SH
    HURWITZ, J
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) : 5672 - 5676
  • [43] Proliferating cell nuclear antigen restores the enzymatic activity of a DNA ligase I deficient in DNA binding
    Trasvina-Arenas, Carlos H.
    Cardona-Felix, Cesar S.
    Azuara-Liceaga, Elisa
    Diaz-Quezada, Corina
    Brieba, Luis G.
    FEBS OPEN BIO, 2017, 7 (05): : 659 - 674
  • [44] Tobacco proliferating cell nuclear antigen binds directly and stimulates both activity and processivity of ddNTP-sensitive mungbean DNA polymerase
    Roy, Sujit
    Choudhury, Swarup Roy
    Mukherjee, Sunil K.
    Sengupta, Dibyendu N.
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2007, 468 (01) : 22 - 31
  • [45] DNA ploidy and proliferating cell nuclear antigen in islet cell tumors
    Tomita, T
    PANCREAS, 1996, 12 (01) : 36 - 47
  • [46] PROLIFERATING CELL NUCLEAR ANTIGEN IS REQUIRED FOR DNA EXCISION REPAIR
    SHIVJI, MKK
    KENNY, MK
    WOOD, RD
    CELL, 1992, 69 (02) : 367 - 374
  • [47] NEDDylation antagonizes ubiquitination of proliferating cell nuclear antigen and regulates the recruitment of polymerase η in response to oxidative DNA damage
    Guan, Junhong
    Yu, Shuyu
    Zheng, Xiaofeng
    PROTEIN & CELL, 2018, 9 (04) : 365 - 379
  • [48] Direct interaction of proliferating cell nuclear antigen with the p125 catalytic subunit of mammalian DNA polymerase δ
    Zhang, P
    Mo, JY
    Perez, A
    Leon, A
    Liu, L
    Mazloum, N
    Xu, H
    Lee, MYWT
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) : 26647 - 26653
  • [49] Human DNA Polymerase β, but Not λ, Can Bypass a 2-Deoxyribonolactone Lesion Together with Proliferating Cell Nuclear Antigen
    Crespan, Emmanuele
    Pasi, Emanuela
    Imoto, Shuhei
    Huebscher, Ulrich
    Greenberg, Marc M.
    Maga, Giovanni
    ACS CHEMICAL BIOLOGY, 2013, 8 (02) : 336 - 344
  • [50] Methylation of DNA polymerase β by protein arginine methyltransferase 1 regulates its binding to proliferating cell nuclear antigen
    El-Andaloussi, Nazim
    Valovka, Taras
    Toueille, Magali
    Hassa, Paul O.
    Gehrig, Peter
    Covic, Marcela
    Huebscher, Ulrich
    Hottiger, Michael O.
    FASEB JOURNAL, 2007, 21 (01): : 26 - 34