Department of Biological Sciences, Idaho State University, Pocatello, ID, USA.
FEMS Microbiol Ecol. 2010 Jun;72(3):343-53. doi: 10.1111/j.1574-6941.2010.00868.x.
Two different versions of the 16S rRNA gene, one of which contained an unusual 100-bp insertion in helix 6, were detected in isolate UFO1 acquired from the Oak Ridge Integrated Field-Research Challenge (ORIFRC) site in Tennessee. rRNA was extracted from UFO1 and analyzed by reverse transcriptase-quantitative PCR with insert- and non-insert-specific primers; only the noninsert 16S rRNA gene sequence was detected. Similarly, PCR-based screening of a cDNA library (190 clones) constructed from reverse-transcribed rRNA from UFO1 did not detect any clones containing the 100-bp insert. Examination of cDNA with primers specific to the insert-bearing 16S rRNA gene, but downstream of the insert, suggests that the insert was excised from rRNA. Inspection of other 16S rRNA genes in the GenBank database revealed that a homologous insert sequence, also found in helix 6, has been reported in other environmental clones, including those acquired from ORIFRC enrichments. These findings demonstrate the existence of widely divergent copies of the 16S rRNA gene within the same organism, which may confound 16S rRNA gene-based methods of estimating microbial diversity in environmental samples.
从田纳西州橡树岭综合野外研究挑战 (ORIFRC) 现场获得的分离株 UFO1 中检测到两个不同版本的 16S rRNA 基因,其中一个在螺旋 6 中包含一个不寻常的 100bp 插入。从 UFO1 中提取 rRNA,并使用插入和非插入特异性引物通过逆转录定量 PCR 进行分析;仅检测到非插入的 16S rRNA 基因序列。同样,从 UFO1 的反转录 rRNA 构建的 cDNA 文库(190 个克隆)的基于 PCR 的筛选未检测到任何包含 100bp 插入的克隆。用针对带有插入的 16S rRNA 基因但位于插入下游的引物检查 cDNA 表明插入已从 rRNA 中切除。检查 GenBank 数据库中的其他 16S rRNA 基因表明,在其他环境克隆中也发现了一个同源的插入序列,也在螺旋 6 中,包括从 ORIFRC 富集物中获得的克隆。这些发现表明,同一生物体中存在广泛差异的 16S rRNA 基因拷贝,这可能会混淆基于 16S rRNA 基因的方法来估计环境样品中的微生物多样性。