A Conserved Histophilus somni 23S Intervening Sequence Yields Functional, Fragmented 23S rRNA

被引:0
作者
Harhay, Gregory P. [1 ]
Harhay, Dayna M. [1 ]
Brader, Kerry D. [1 ]
Smith, Timothy P. L. [1 ]
机构
[1] ARS, USDA, US Meat Anim Res Ctr, Clay Ctr, NE 68933 USA
来源
MICROBIOLOGY SPECTRUM | 2021年 / 9卷 / 03期
关键词
23S RNA; DNA sequencing; Pasteurellaceae; RNA stability; RNA structure; cattle; genomics; Gram-negative bacteria; intervening sequence; mucosal pathogens; transcription; bovine respiratory disease; VIRUS; GS-5734; DISCOVERY; INHIBITOR; EFFICACY; PRODRUGS; EBOLA; CELLS;
D O I
10.1128/Spectrum.01431-21
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Histophilus somni is a Gram-negative bacterial organism that acts as an opportunistic pathogen and is a fastidious member of the Pasteurellaceae family associated with diseases of respiratory, reproductive, cardiac, and other tissues of ruminants. We identified an intervening sequence (IVS) embedded in all five copies of the 23S rRNA gene in the closed genome sequence of the H. somni isolate USDA-ARS-USMARC-63250 that may play an important role in affecting the biology of the organism. Sequencing the RNA from this isolate shows that most of the IVS is cleaved from the transcript, resulting in independent fragments of this structural rRNA that remain functional within the bacterial ribosome. The IVS lies between positions 1170 and 1278 bp of the 3,017-bp gene and exhibits self-complementarity between its 5 ' and 3 ' ends that predicts a stem-loop structure interrupting helix-45 in the transcribed 23S rRNA. Excision removes a 94-nucleotide (nt) stem-loop structure that displays an unusual 1-nt 3 ' end overhang instead of the more typical 2-nt overhang commonly observed at the ends of other excised IVS stem-loops. A comparison with genomes of other H. somni isolates indicates that this IVS is highly conserved, with 31 of 32 complete genomes having similar interruptions of canonical 23S rRNA genes. The potential biological effects of either the released IVS or the fragmentation of the functional 23S rRNA are unknown, but fragmentation may enhance rRNA degradation in ways that contribute to the regulation of gene expression.
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