Suppr超能文献

通过组合随机相位基因组测序和抑制性消减杂交揭示的黄化瘤胃球菌FD-1的菌株特异性基因组区域

Strain-specific genomic regions of Ruminococcus flavefaciens FD-1 as revealed by combinatorial random-phase genome sequencing and suppressive subtractive hybridization.

作者信息

Antonopoulos Dionysios A, Nelson Karen E, Morrison Mark, White Bryan A

机构信息

Department of Animal Sciences, University of Illinois at Urbana-Champaign, 1207 West Gregory Dr, Urbana, IL 61801, USA.

出版信息

Environ Microbiol. 2004 Apr;6(4):335-46. doi: 10.1111/j.1462-2920.2004.00576.x.

Abstract

Two closely related strains of the Gram-positive, cellulolytic ruminal bacterium Ruminococcus flavefaciens were compared at the genomic level by suppressive subtractive hybridization. The two strains investigated in this study differ by 1.94% in their respective 16S rDNA genes. Three hundred and eighty-four PCR-amplified products were cloned and then screened for their strain identity by dot blot hybridization. Based on redundancy percentages of the clones sequenced, 9.5% of the genome of the R. flavefaciens FD-1 strain is not present in the JM1 strain. The majority of identities of individual cloned subtracted products (642 bp average length) bore no relation to deposited sequences in GenBank (42% of the subtracted library), whereas of those with putative assigned functions 7% are loosely associated with fibre-degradation, 6% with insertion elements, transposons and phage-like ORFs, 5% with cell membrane associated proteins and 3% with signal transduction. Subtracted sequences were then supplemented with the draft (2 x coverage) genome sequence of R. flavefaciens FD-1 to indicate potential regions of rearrangement within the genome, including a novel insertion sequence.

摘要

通过抑制性消减杂交技术,在基因组水平上比较了革兰氏阳性、纤维素分解瘤胃细菌黄化瘤胃球菌的两个密切相关菌株。本研究中所研究的两个菌株在各自的16S rDNA基因上存在1.94%的差异。对384个PCR扩增产物进行克隆,然后通过斑点杂交筛选其菌株同一性。根据所测序克隆的冗余百分比,黄化瘤胃球菌FD-1菌株基因组的9.5%在JM1菌株中不存在。单个克隆的消减产物(平均长度642 bp)的大多数同一性与GenBank中已存序列无关(占消减文库的42%),而那些具有推定功能的产物中,7%与纤维降解松散相关,6%与插入元件、转座子和噬菌体样开放阅读框相关,5%与细胞膜相关蛋白相关,3%与信号转导相关。然后,将消减序列与黄化瘤胃球菌FD-1的草图基因组序列(2倍覆盖)进行补充,以指示基因组内潜在的重排区域,包括一个新的插入序列。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验