Gene orders in the upstream of 16S rRNA genes divide genera of the family Halobacteriaceae into two groups

被引:27
|
作者
Minegishi, Hiroaki [1 ]
Kamekura, Masahiro [2 ]
Kitajima-Ihara, Tomomi [3 ]
Nakasone, Kaoru [4 ]
Echigo, Akinobu [1 ,5 ]
Shimane, Yasuhiro [6 ]
Usami, Ron [1 ,5 ,6 ]
Itoh, Takashi [7 ]
Ihara, Kunio [3 ]
机构
[1] Toyo Univ, Bionano Elect Res Ctr, Kawagoe, Saitama, Japan
[2] Halophiles Res Inst, Noda, Chiba, Japan
[3] Nagoya Univ, Ctr Gene Res, Nagoya, Aichi 46401, Japan
[4] Kinki Univ, Sch Engn, Dept Chem & Environm Technol, Hiroshima, Japan
[5] Toyo Univ, Fac Sci & Engn, Kawagoe, Saitama, Japan
[6] Toyo Univ, Grad Sch Interdisciplinary New Sci, Kawagoe, Saitama, Japan
[7] RIKEN, BioResource Ctr, Wako, Saitama, Japan
关键词
HALOPHILIC ARCHAEON; GENOME SEQUENCE; SP; NOV; EVOLUTION; HALOARCULA; PHYLOGENY; RPOB'; HETEROGENEITY; TRANSCRIPTION;
D O I
10.1099/ijs.0.031708-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In many prokaryotic species, 16S rRNA genes are present in multiple copies, and their sequences in general do not differ significantly owing to concerted evolution. At the time of writing, the genus Haloarcula of the family Halobacteriaceae comprises nine species with validly published names, all of which possess two to four highly heterogeneous 16S rRNA genes. Existence of multiple heterogeneous 16S rRNA genes makes it difficult to reconstruct a biological phylogenetic tree using their sequence data. If the orthologous gene is able to be discriminated from paralogous genes, a tree reconstructed from orthologous genes will reflect a simple biological phylogenetic relationship. At present, however, we have no means to distinguish the orthologous rRNA operon from paralogous ones in the members of the family Halobacteriaceae. In this study, we found that the dihydroorotate oxidase gene, pyrD, was present in the immediate upstream of one 16S rRNA gene in each of ten strains of the family Halobacteriaceae whose genome sequences have been determined, and the direction of the pyrD gene was opposite to that of the 16S rRNA genes. In two other strains whose genome sequences have been determined, the pyrD gene was present in far separated positions. We designed PCR primer sets to amplify DNA fragments encompassing a region from the conserved region of the pyrD gene to a conserved region of the tRNA-Ala gene or the 23S rRNA gene to determine the 16S rRNA gene sequences preceded by the pyrD gene, and to see if the pyrD gene is conserved in the immediate upstream of rRNA operon(s) in the type strains of the type species of 28 genera of the family Halobacteriaceae. Seventeen type strains, including the ten strains mentioned above, gave amplified DNA fragments of approximately 4000 bp, while eleven type strains, including the two strains mentioned above, did not give any PCR products. These eleven strains are members of the Clade I haloarchaea, originally defined by Walsh et al. (2004) and expanded by Minegishi et al. (2010). Analysis of contig sequences of three strains belonging to the Clade I haloarchaea also revealed the absence of the pyrD gene in the immediate upstream of any 16S rRNA genes. It may be scientifically sound to hypothesize that during the evolution of members of the family Halobacteriaceae, a pyrD gene transposition event happened in one group and this was followed by subsequent speciation processes in each group, yielding species/genera of the Clade I group and the rest' of the present family Halobacteriaceae.
引用
收藏
页码:188 / 195
页数:8
相关论文
共 50 条
  • [31] Phylogeny of the Mycoplasma mycoides cluster as determined by sequence analysis of the 16S rRNA genes from the two rRNA operons
    Pettersson, B
    Leitner, T
    Ronaghi, M
    Bolske, G
    Uhlen, M
    Johansson, KE
    JOURNAL OF BACTERIOLOGY, 1996, 178 (14) : 4131 - 4142
  • [32] Critical evaluation of two primers commonly used for amplification of bacterial 16S rRNA genes
    Frank, Jeremy A.
    Reich, Claudia I.
    Sharma, Shobha
    Weisbaum, Jon S.
    Wilson, Brenda A.
    Olsen, Gary J.
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (08) : 2461 - 2470
  • [33] Patterns of sequence variation in two regions of the 16S rRNA multigene family of Escherichia coli
    Martínez-Murcia, AJ
    Antón, AI
    Rodríguez-Valera, F
    INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1999, 49 : 601 - 610
  • [34] Latitudinal variation in the potential activity of Atlantic Ocean bacterioplankton revealed through 16S rRNA and 16S rRNA gene metabarcoding
    Allen, Ro
    Bird, Kimberley E.
    Murrell, J. Colin
    Cunliffe, Michael
    FRONTIERS IN MARINE SCIENCE, 2023, 10
  • [35] Activity profiles for marine sponge-associated bacteria obtained by 16S rRNA vs 16S rRNA gene comparisons
    Janine Kamke
    Michael W Taylor
    Susanne Schmitt
    The ISME Journal, 2010, 4 : 498 - 508
  • [36] Copy number of the 16S rRNA gene in Coxiella burnetii
    Afseth, G
    Mallavia, LP
    EUROPEAN JOURNAL OF EPIDEMIOLOGY, 1997, 13 (06) : 729 - 731
  • [37] Activity profiles for marine sponge-associated bacteria obtained by 16S rRNA vs 16S rRNA gene comparisons
    Kamke, Janine
    Taylor, Michael W.
    Schmitt, Susanne
    ISME JOURNAL, 2010, 4 (04): : 498 - 508
  • [38] Intravaginal microbial flora by the 16S rRNA gene sequencing
    Yoshimura, Kazuaki
    Morotomi, Nobuo
    Fukuda, Kazumasa
    Nakano, Masahiro
    Kashimura, Masamichi
    Hachisuga, Toru
    Taniguchi, Hatsumi
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2011, 205 (03) : 235.e1 - 235.e9
  • [39] Genetic environment of 16S rRNA methylase gene rmtD
    Doi, Yohei
    Adams-Haduch, Jennifer M.
    Paterson, David L.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (06) : 2270 - 2272
  • [40] Transcriptional analysis of the 16S rRNA gene in Rickettsia prowazekii
    Pang, HL
    Winkler, HH
    JOURNAL OF BACTERIOLOGY, 1996, 178 (06) : 1750 - 1755