Widespread stop-codon recoding in bacteriophages may regulate translation of lytic genes

被引:28
作者
Borges, Adair L. [1 ,2 ]
Lou, Yue Clare [1 ,3 ]
Sachdeva, Rohan [1 ,4 ]
Al-Shayeb, Basem [1 ,3 ]
Penev, Petar, I [4 ]
Jaffe, Alexander L. [3 ]
Lei, Shufei [4 ]
Santini, Joanne M. [5 ]
Banfield, Jillian F. [1 ,2 ,4 ,6 ,7 ]
机构
[1] Univ Calif Berkeley, Innovat Genom Inst, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Environm Sci Policy & Management, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Earth & Planetary Sci, Berkeley, CA 94720 USA
[5] UCL, Dept Struct & Mol Biol, Div Biosci, London, England
[6] Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[7] Univ Melbourne, Parkville, Vic, Australia
关键词
TRYPTOPHAN CODON; PREMATURE LYSIS; TRANSFER-RNA; PROTEIN; ALIGNMENT; UGA; SEQUENCE; PHAGE; READ; SELENOCYSTEINE;
D O I
10.1038/s41564-022-01128-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Computational analyses reveal widespread recoding in gut phages, which is hypothesized to control timing of lysis. Bacteriophages (phages) are obligate parasites that use host bacterial translation machinery to produce viral proteins. However, some phages have alternative genetic codes with reassigned stop codons that are predicted to be incompatible with bacterial translation systems. We analysed 9,422 phage genomes and found that stop-codon recoding has evolved in diverse clades of phages that infect bacteria present in both human and animal gut microbiota. Recoded stop codons are particularly over-represented in phage structural and lysis genes. We propose that recoded stop codons might function to prevent premature production of late-stage proteins. Stop-codon recoding has evolved several times in closely related lineages, which suggests that adaptive recoding can occur over very short evolutionary timescales.
引用
收藏
页码:918 / +
页数:19
相关论文
共 77 条
  • [71] UGA IS READ AS TRYPTOPHAN IN MYCOPLASMA-CAPRICOLUM
    YAMAO, F
    MUTO, A
    KAWAUCHI, Y
    IWAMI, M
    IWAGAMI, S
    AZUMI, Y
    OSAWA, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (08) : 2306 - 2309
  • [72] Degradation of host translational machinery drives tRNA acquisition in viruses
    Yang, Joy Y.
    Fang, Wenwen
    Miranda-Sanchez, Fabiola
    Brown, Julia M.
    Kauffman, Kathryn M.
    Acevero, Chantel M.
    Bartel, David P.
    Polz, Martin F.
    Kelly, Libusha
    [J]. CELL SYSTEMS, 2021, 12 (08) : 771 - +
  • [73] Phage Lysis: Three Steps, Three Choices, One Outcome
    Young, Ryland
    [J]. JOURNAL OF MICROBIOLOGY, 2014, 52 (03) : 243 - 258
  • [74] Analysis of metagenome-assembled viral genomes from the human gut reveals diverse putative CrAss-like phages with unique genomic features
    Yutin, Natalya
    Benler, Sean
    Shmakov, Sergei A.
    Wolf, Yuri, I
    Tolstoy, Igor
    Rayko, Mike
    Antipov, Dmitry
    Pevzner, Pavel A.
    Koonin, Eugene, V
    [J]. NATURE COMMUNICATIONS, 2021, 12 (01)
  • [75] Decision Making at a Subcellular Level Determines the Outcome of Bacteriophage Infection
    Zeng, Lanying
    Skinner, Samuel O.
    Zong, Chenghang
    Sippy, Jean
    Feiss, Michael
    Golding, Ido
    [J]. CELL, 2010, 141 (04) : 682 - 691
  • [76] A Completely Reimplemented MPI Bioinformatics Toolkit with a New HHpred Server at its Core
    Zimmermann, Lukas
    Stephens, Andrew
    Nam, Seung-Zin
    Rau, David
    Kuebler, Jonas
    Lozajic, Marko
    Gabler, Felix
    Soeding, Johannes
    Lupas, Andrei N.
    Alva, Vikram
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2018, 430 (15) : 2237 - 2243
  • [77] COTRANSLATIONAL INSERTION OF SELENOCYSTEINE INTO FORMATE DEHYDROGENASE FROM ESCHERICHIA-COLI DIRECTED BY A UGA CODON
    ZINONI, F
    BIRKMANN, A
    LEINFELDER, W
    BOCK, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) : 3156 - 3160