Identification of Rv3852 as a nucleoid-associated protein in Mycobacterium tuberculosis

被引:16
|
作者
Werlang, Isabel C. R. [1 ,2 ]
Schneider, Cristopher Z. [1 ]
Mendonca, Jordana D. [1 ]
Palma, Mario S. [3 ]
Basso, Luiz A. [1 ]
Santos, Diogenes S. [1 ]
机构
[1] Pontificia Univ Catolica Rio Grande do Sul, Inst Nacl Ciencia & Tecnol Tuberculose, Ctr Pesquisas Biol Mol & Func, BR-90619900 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Programa Posgrad Biol Celular & Mol, BR-91501970 Porto Alegre, RS, Brazil
[3] Univ Estadual Paulista, Inst Biociencias, Ctr Estudos Insetos Sociais, Lab Biol Estrutural & Zooquim,Dept Biol, BR-13506900 Rio Claro, SP, Brazil
来源
MICROBIOLOGY-SGM | 2009年 / 155卷
关键词
HISTONE-LIKE PROTEIN; VIRULENCE GENE-EXPRESSION; DNA-BINDING PROTEIN; H-NS; ESCHERICHIA-COLI; CURVED DNA; ARCHITECTURAL ROLE; STATIONARY-PHASE; CHROMATIN; LSR2;
D O I
10.1099/mic.0.030148-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tuberculosis remains the major cause of mortality due to a bacterial pathogen, Mycobacterium tuberculosis. The molecular mechanisms of infection and persistence have not been completely elucidated for this pathogen. Studies involving nucleoid-associated proteins (NAPs), which have been related to the control and influence of virulence genes in pathogenic bacteria, can help unveil the virulence process of M. tuberculosis. Here, we describe the initial characterization of an ORF for an M. tuberculosis putative NAP. The Rv3852 gene was cloned and expressed, and its product purified to homogeneity. A qualitative protein-DNA binding assay was carried out by gel-retardation and the protein affinity for specific DNA sequences was assessed quantitatively by surface plasmon resonance (SPR). A stoichiometry of 10 molecules of monomeric protein per molecule of DNA was determined. The monophasic apparent dissociation rate constant values increased to a saturable level as a function of protein concentration, yielding two limiting values for the molecular recognition of proU2 DNA. A protein-DNA binding mechanism is proposed. In addition, functional complementation studies with an Escherichia coli has mutant reinforce the likelihood that the Rv3852 protein represents a novel NAP in M. tuberculosis.
引用
收藏
页码:2652 / 2663
页数:12
相关论文
共 50 条
  • [1] Identification of Rv3852 as an Agrimophol-Binding Protein in Mycobacterium tuberculosis
    Zhao, Nan
    Sun, Mingna
    Burns-Huang, Kristin
    Jiang, Xiuju
    Ling, Yan
    Darby, Crystal
    Ehrt, Sabine
    Liu, Gang
    Nathan, Carl
    PLOS ONE, 2015, 10 (05):
  • [2] Rv3852 (H-NS) of Mycobacterium tuberculosis Is Not Involved in Nucleoid Compaction and Virulence Regulation
    Odermatt, Nina T.
    Sala, Claudia
    Benjak, Andrej
    Kolly, Gaelle S.
    Vocat, Anthony
    Lupien, Andreanne
    Cole, Stewart T.
    JOURNAL OF BACTERIOLOGY, 2017, 199 (16)
  • [3] Direct Interaction of Polar Scaffolding Protein Wag31 with Nucleoid-Associated Protein Rv3852 Regulates Its Polar Localization
    Garg, Rajni
    Anand, Chinmay
    Ganguly, Sohini
    Rao, Sandhya
    Verma, Rinkee
    Nagaraja, Valakunja
    CELLS, 2021, 10 (06)
  • [4] Identification of Rv3852 as an Agrimophol-Binding Protein in Mycobacterium tuberculosis (vol 10, e0126211, 2015)
    Zhao, N.
    Sun, M.
    Burns-Huang, K.
    Jiang, X.
    Ling, Y.
    Darby, C.
    PLOS ONE, 2015, 10 (06):
  • [5] Virulence Regulator EspR of Mycobacterium tuberculosis Is a Nucleoid-Associated Protein
    Blasco, Benjamin
    Chen, Jeffrey M.
    Hartkoorn, Ruben
    Sala, Claudia
    Uplekar, Swapna
    Rougemont, Jacques
    Pojer, Florence
    Cole, Stewart T.
    PLOS PATHOGENS, 2012, 8 (03)
  • [6] The heparin-binding hemagglutinin protein of Mycobacterium tuberculosis is a nucleoid-associated protein
    Keshavam, Chetkar Chandra
    Naz, Saba
    Gupta, Aanchal
    Sanyal, Priyadarshini
    Kochar, Manisha
    Gangwal, Aakriti
    Sangwan, Nitika
    Kumar, Nishant
    Tyagi, Ekta
    Goel, Simran
    Singh, Nitesh Kumar
    Sowpati, Divya Tej
    Khare, Garima
    Ganguli, Munia
    Raze, Dominique
    Locht, Camille
    Basu-Modak, Sharmila
    Gupta, Meetu
    Nandicoori, Vinay Kumar
    Singh, Yogendra
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2023, 299 (12)
  • [7] A novel nucleoid-associated protein of Mycobacterium tuberculosis is a sequence homolog of GroEL
    Basu, Debashree
    Khare, Garima
    Singh, Shashi
    Tyagi, Anil
    Khosla, Sanjeev
    Mande, Shekhar C.
    NUCLEIC ACIDS RESEARCH, 2009, 37 (15) : 4944 - 4954
  • [8] HupB, a Nucleoid-Associated Protein of Mycobacterium tuberculosis, Is Modified by Serine/Threonine Protein Kinases In Vivo
    Gupta, Meetu
    Sajid, Andaleeb
    Sharma, Kirti
    Ghosh, Soumitra
    Arora, Gunjan
    Singh, Ramandeep
    Nagaraja, Valakunja
    Tandon, Vibha
    Singh, Yogendra
    JOURNAL OF BACTERIOLOGY, 2014, 196 (14) : 2646 - 2657
  • [9] Novel stilbene scaffolds efficiently target Mycobacterium tuberculosis nucleoid-associated protein, HU
    Peraman, Ramalingam
    Meka, Geethavani
    Chilamakuru, Naresh Babu
    Kutagulla, Vinay Kumar
    Malla, Saloni
    Ashby, Charles R., Jr.
    Tiwari, Amit K.
    Yiragamreddy, Padmanabha Reddy
    NEW JOURNAL OF CHEMISTRY, 2021, 45 (24) : 10683 - 10692
  • [10] Targeting Mycobacterium tuberculosis nucleoid-associated protein HU with structure-based inhibitors
    Tuhin Bhowmick
    Soumitra Ghosh
    Karuna Dixit
    Varsha Ganesan
    Udupi A. Ramagopal
    Debayan Dey
    Siddhartha P. Sarma
    Suryanarayanarao Ramakumar
    Valakunja Nagaraja
    Nature Communications, 5