Evidence for Moonlighting Functions of the θ Subunit of Escherichia coli DNA Polymerase III

被引:4
|
作者
Dietrich, M. [2 ]
Pedro, L. [2 ]
Garcia, J. [3 ]
Pons, M. [4 ]
Huettener, M. [2 ]
Paytubi, S. [1 ]
Madrid, C. [1 ]
Juarez, A. [1 ,2 ]
机构
[1] Univ Barcelona, Fac Biol, Dept Microbiol, Barcelona, Spain
[2] Inst Bioengn Catalonia IBEC, Barcelona, Spain
[3] Inst Biomed Res, Barcelona, Spain
[4] Univ Barcelona, Dept Organ Chem, Lab Biomol NMR, Barcelona, Spain
关键词
H-NS; EPSILON-SUBUNIT; PROOFREADING EXONUCLEASE; YERSINIA-ENTEROCOLITICA; ALPHA-SUBUNIT; GENE-PRODUCT; HOT GENE; HHA; PROTEINS; EXPRESSION;
D O I
10.1128/JB.01448-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The holE gene is an enterobacterial ORFan gene (open reading frame [ORF] with no detectable homology to other ORFs in a database). It encodes the theta subunit of the DNA polymerase III core complex. The precise function of the theta subunit within this complex is not well established, and loss of holE does not result in a noticeable phenotype. Paralogs of holE are also present on many conjugative plasmids and on phage P1 (hot gene). In this study, we provide evidence indicating that theta (HolE) exhibits structural and functional similarities to a family of nucleoid-associated regulatory proteins, the Hha/YdgT-like proteins that are also encoded by enterobacterial ORFan genes. Microarray studies comparing the transcriptional profiles of Escherichia coli holE, hha, and ydgT mutants revealed highly similar expression patterns for strains harboring holE and ydgT alleles. Among the genes differentially regulated in both mutants were genes of the tryptophanase (tna) operon. The tna operon consists of a transcribed leader region, tnaL, and two structural genes, tnaA and tnaB. Further experiments with transcriptional lacZ fusions (tnaL::lacZ and tnaA::lacZ) indicate that HolE and YdgT downregulate expression of the tna operon by possibly increasing the level of Rho-dependent transcription termination at the tna operon's leader region. Thus, for the first time, a regulatory function can be attributed to HolE, in addition to its role as structural component of the DNA polymerase III complex.
引用
收藏
页码:1102 / 1112
页数:11
相关论文
共 50 条
  • [1] Structure of the θ subunit of Escherichia coli DNA polymerase III in complex with the ε subunit
    Keniry, Max A.
    Park, Ah Young
    Owen, Elisabeth A.
    Hamdan, Samir M.
    Pintacuda, Guido
    Otting, Gottfried
    Dixon, Nicholas E.
    JOURNAL OF BACTERIOLOGY, 2006, 188 (12) : 4464 - 4473
  • [2] The θ subunit of Escherichia coli DNA polymerase III:: a role in stabilizing the ε proofreading subunit
    Taft-Benz, SA
    Schaaper, RM
    JOURNAL OF BACTERIOLOGY, 2004, 186 (09) : 2774 - 2780
  • [3] The proofreading exonuclease subunit of Escherichia coli DNA polymerase III is tethered to the polymerase subunit via a flexible linker
    Ozawa, Kiyoshi
    Jergic, Slobodan
    Park, Ah Young
    Dixon, Nicholas E.
    Otting, Gottfried
    NUCLEIC ACIDS RESEARCH, 2008, 36 (15) : 5074 - 5082
  • [4] Mutator mutants of Escherichia coli carrying a defect in the DNA polymerase III τ subunit
    Pham, PT
    Zhao, W
    Schaaper, RM
    MOLECULAR MICROBIOLOGY, 2006, 59 (04) : 1149 - 1161
  • [5] Mechanism of β clamp opening by the δ subunit of Escherichia coli DNA polymerase III holoenzyme
    Stewart, J
    Hingorani, MM
    Kelmann, Z
    O'Donnell, M
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) : 19182 - 19189
  • [6] NMR solution structure of the θ subunit of DNA polymerase III from Escherichia coli
    Keniry, MA
    Berthon, HA
    Yang, JY
    Miles, CS
    Dixon, NE
    PROTEIN SCIENCE, 2000, 9 (04) : 721 - 733
  • [7] Elucidation of the ε-θ subunit interface of Escherichia coli DNA polymerase III by NMR spectroscopy
    DeRose, EF
    Darden, T
    Harvey, S
    Gabel, S
    Perrino, FW
    Schaaper, RM
    London, RE
    BIOCHEMISTRY, 2003, 42 (13) : 3635 - 3644
  • [8] A preliminary CD and NMR study of the Escherichia coli DNA polymerase III Θ subunit
    Li, DW
    Allen, DL
    Harvey, S
    Perrino, FW
    Schaaper, RM
    London, RE
    PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 1999, 36 (01) : 111 - 116
  • [9] Solution structure of Domains IVa and V of the τ subunit of Escherichia coli DNA polymerase III and interaction with the α subunit
    Su, Xun-Cheng
    Jergic, Slobodan
    Keniry, Max A.
    Dixon, Nicholas E.
    Otting, Gottfried
    NUCLEIC ACIDS RESEARCH, 2007, 35 (09) : 2825 - 2832
  • [10] Fidelity and error specificity of the alpha catalytic subunit of Escherichia coli DNA polymerase III
    Mo, JY
    Schaaper, RM
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) : 18947 - 18953