Yeast mitochondrial RNA polymerase primes mitochondrial DNA polymerase at origins of replication and promoter sequences

被引:15
作者
Sanchez-Sandoval, Eugenia [1 ]
Diaz-Quezada, Corina [1 ]
Velazquez, Gilberto [1 ]
Arroyo-Navarro, Luis F. [1 ]
Almanza-Martinez, Norineli [1 ]
Trasvina-Arenas, Carlos H. [1 ]
Brieba, Luis G. [1 ]
机构
[1] IPN, Ctr Invest & Estudios Avanzados, Lab Nacl Genom Biodiversidad, Guanajuato 36500, Mexico
基金
芬兰科学院;
关键词
Replication; Yeast mitochondria; In vitro; RPO41; BACTERIOPHAGE-T7; DEOXYRIBONUCLEIC-ACID; N-TERMINAL DOMAIN; SACCHAROMYCES-CEREVISIAE; IN-VITRO; HYPERSUPPRESSIVE PETITE; BIASED INHERITANCE; SPECIFICITY FACTOR; PURIFIED PROTEINS; BINDING-PROTEIN; WILD-TYPE;
D O I
10.1016/j.mito.2015.06.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Three proteins phylogenetically grouped with proteins from the T7 replisome localize to yeast mitochondria: DNA polymerase gamma (Mip1), mitochondrial RNA polymerase (Rpo41), and a single-stranded binding protein (Rim1). Human and T7 bacteriophage RNA polymerases synthesize primers for their corresponding DNA polymerases. In contrast, DNA replication in yeast mitochondria is explained by two models: a transcription-dependent model in which Rpo41 primes Mip1 and a model in which double stranded breaks create free 3' OHs that are extended by Mip1. Herein we found that Rpo41 transcribes RNAs that can be extended by Mip1 on single and double-stranded DNA. In contrast to human mitochondrial RNA polymerase, which primes DNA polymerase gamma using transcripts from the light-strand and heavy-strand origins of replication, Rpo41 primes Mip1 at replication origins and promoter sequences in vitro. Our results suggest that in ori1, short transcripts serve as primers, whereas in ori5 an RNA transcript longer than 29 nucleotides is used as primer. (C) 2015 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
引用
收藏
页码:22 / 31
页数:10
相关论文
共 50 条
  • [31] Proficient Replication of the Yeast Genome by a Viral DNA Polymerase
    Stodola, Joseph L.
    Stith, Carrie M.
    Burgers, Peter M.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (22) : 11698 - 11705
  • [32] C-Terminal Extension of the Yeast Mitochondrial DNA Polymerase Determines the Balance between Synthesis and Degradation
    Viikov, Katrin
    Jasnovidova, Olga
    Tamm, Tiina
    Sedman, Juhan
    PLOS ONE, 2012, 7 (03):
  • [33] Mitochondrial Disorders of DNA Polymerase γ Dysfunction From Anatomic to Molecular Pathology Diagnosis
    Zhang, Linsheng
    Chan, Sherine S. L.
    Wolff, Daynna J.
    ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2011, 135 (07) : 925 - 934
  • [34] Structural origins of Escherichia coli RNA polymerase open promoter complex stability
    Saecker, Ruth M.
    Chen, James
    Chiu, Courtney E.
    Malone, Brandon
    Sotiris, Johanna
    Ebrahim, Mark
    Yen, Laura Y.
    Eng, Edward T.
    Darst, Seth A.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2021, 118 (40)
  • [35] Cryo-EM Structures Reveal Transcription Initiation Steps by Yeast Mitochondrial RNA Polymerase
    De Wijngaert, Brent
    Sultana, Shemaila
    Singh, Anupam
    Dharia, Chhaya
    Vanbuel, Hans
    Shen, Jiayu
    Vasilchuk, Daniel
    Martinez, Sergio E.
    Kandiah, Eaazhisai
    Patel, Smita S.
    Das, Kalyan
    MOLECULAR CELL, 2021, 81 (02) : 268 - +
  • [36] Autoregulation of an RNA polymerase II promoter by the RNA polymerase III transcription factor III C (TFIIIC) complex
    Kleinschmidt, Richard A.
    LeBlanc, Kimberly E.
    Donze, David
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (20) : 8385 - 8389
  • [37] Modeling of pathogenic variants of mitochondrial DNA polymerase: insight into the replication defects and implication for human disease
    Hoyos-Gonzalez, Nallely
    Trasvina-Arenas, Carlos H.
    Degiorgi, Andrea
    Castro-Lara, Atzimaba Y.
    Peralta-Castro, Antolin
    Jimenez-Sandoval, Pedro
    Diaz-Quezada, Corina
    Lodi, Tiziana
    Baruffini, Enrico
    Brieba, Luis G.
    BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2020, 1864 (07):
  • [38] PCNA binding domains in all three subunits of yeast DNA polymerase δ modulate its function in DNA replication
    Acharya, Narottam
    Klassen, Roland
    Johnson, Robert E.
    Prakash, Louise
    Prakash, Satya
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (44) : 17927 - 17932
  • [39] Assembly and Cryo-EM structure determination of yeast mitochondrial RNA polymerase initiation complex intermediates
    Martinez, Sergio E.
    Singh, Anupam
    De Wijngaert, Brent
    Sultana, Shemaila
    Dharia, Chhaya
    Vanbuel, Hans
    Shen, Jiayu
    Vasilchuk, Daniel
    Patel, Smita S.
    Das, Kalyan
    STAR PROTOCOLS, 2021, 2 (02):
  • [40] Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA
    Corbi, Daniel
    Amon, Angelika
    PLOS GENETICS, 2021, 17 (10):