Intragenomic 16S rDNA divergence in Haloarcula marismortui is an adaptation to different temperatures

被引:70
|
作者
Lopez-Lopez, A. [1 ]
Benlloch, S. [2 ]
Bonfa, M. [1 ]
Rodriguez-Valera, F. [1 ]
Mira, A. [1 ]
机构
[1] Univ Miguel Hernandez, Div Microbiol, Evolutionary Genom Grp, Alacant 03550, Spain
[2] Hosp Gen Univ Alicante, Alacant, Spain
关键词
genome evolution; ribosomal operons; concerted evolution; thermal adaptation; extremophile; thermophile; paralogues; thermal stability; phylogenetic marker; real-time PCR;
D O I
10.1007/s00239-007-9047-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The halophilic archaeon Haloarcula marismortui contains three ribosomal RNA operons, designated rrnA, rrnB, and rrnC. Operons A and C are virtually identical, whereas operon B presents a high divergence in nucleotide sequence, having up to 135 nucleotide polymorphisms among the three 16S, 23S, and 5S ribosomal RNA genes. Quantitative PCR and structural analyses have been performed to elucidate whether the presence of this intragenomic heterogeneity could be an adaptation to the variable environmental conditions in the natural habitat of H. marismortui. Variation in salt concentration did not affect expression but variation in incubation temperature did produce significant changes, with operon B displaying an expression level four times higher than the other two together at 50 degrees C and three times lower at 15 degrees C. We show that the putative promoter region of operon B is also different. In addition, the predicted secondary structure of these genes indicated that they have distinct stabilities at different temperatures and a mutant strain lacking operon B grew slower at high temperatures. This study supports the idea that divergent rRNA genes can be adaptive, with different variants being functional under different environmental conditions (e.g., temperature). The same phenomenon could take place in other halophiles or thermophiles with intragenomic rDNA heterogeneity, where the use of 16S rDNA as a phylogenetic marker and indicator of biodiversity should be used with caution.
引用
收藏
页码:687 / 696
页数:10
相关论文
共 50 条
  • [31] 16S rDNA analysis of osteoporotic rats treated with osteoking
    Sun, Yan
    Zhang, Hui-Jie
    Chen, Ran
    Lee, Wen-Hui
    Zhao, Hong-Bin
    JOURNAL OF MEDICAL MICROBIOLOGY, 2022, 71 (06)
  • [32] FastGroup: A program to dereplicate libraries of 16S rDNA sequences
    Victor Seguritan
    Forest Rohwer
    BMC Bioinformatics, 2
  • [33] 16S rDNA analysis of the intestinal microbes in osteoporotic rats
    Sun, Yan
    Zhang, Hui-Jie
    Chen, Ran
    Zhao, Hong-Bin
    Lee, Wen-Hui
    BIOSCIENCE OF MICROBIOTA FOOD AND HEALTH, 2021, 40 (03) : 156 - 167
  • [34] 香蕉园土壤16S rDNA文库分析
    黄珍
    谭志琼
    阮云泽
    热带作物学报, 2010, (06) : 989 - 993
  • [35] Current Opinion of Microorganism Classification by 16S rDNA Database
    Kim, Myung Kyum
    MOLECULAR & CELLULAR TOXICOLOGY, 2010, 6 (03) : 31 - 31
  • [36] 16S rDNA sequence for Identification and Discriminating Pseudomonas aeruginosa
    Parvathi, J. R.
    Sunita, S. D.
    Vasudha, B. K.
    JOURNAL OF PURE AND APPLIED MICROBIOLOGY, 2010, 4 (02): : 579 - 587
  • [37] 16S rDNA targeted PCR for the detection of Paenibacillus macerans
    Vollú, RE
    dos Santos, SCC
    Seldin, L
    LETTERS IN APPLIED MICROBIOLOGY, 2003, 37 (05) : 415 - 420
  • [38] What is broad-range 16S rDNA PCR?
    Patel, Amani
    Harris, Kathryn A.
    Fitzgerald, Felicity
    ARCHIVES OF DISEASE IN CHILDHOOD-EDUCATION AND PRACTICE EDITION, 2017, 102 (05): : 261 - 264
  • [39] PHYLOGENY OF THE GENUS AZOSPIRILLUM BASED ON 16S RDNA SEQUENCE
    FANI, R
    BANDI, C
    BAZZICALUPO, M
    CECCHERINI, MT
    FANCELLI, S
    GALLORI, E
    GERACE, L
    GRIFONI, A
    MICLAUS, N
    DAMIANI, G
    FEMS MICROBIOLOGY LETTERS, 1995, 129 (2-3) : 195 - 200
  • [40] 16S rDNA sequence analysis of Xylella fastidiosa strains
    Chen, J
    Jarret, RL
    Qin, X
    Hartung, JS
    Banks, D
    Chang, CJ
    Hopkins, DL
    SYSTEMATIC AND APPLIED MICROBIOLOGY, 2000, 23 (03) : 349 - 354