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Compositional biases of bacterial genomes and evolutionary implications.

机译:细菌基因组的组成偏差及其进化意义。

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摘要

We compare and contrast genome-wide compositional biases and distributions of short oligonucleotides across 15 diverse prokaryotes that have substantial genomic sequence collections. These include seven complete genomes (Escherichia coli, Haemophilus influenzae, Mycoplasma genitalium, Mycoplasma pneumoniae, Synechocystis sp. strain PCC6803, Methanococcus jannaschii, and Pyrobaculum aerophilum). A key observation concerns the constancy of the dinucleotide relative abundance profiles over multiple 50-kb disjoint contigs within the same genome. (The profile is rhoXY* = fXY*/fX*fY* for all XY, where fX* denotes the frequency of the nucleotide X and fY* denotes the frequency of the dinucleotide XY, both computed from the sequence concatenated with its inverted complementary sequence.) On the basis of this constancy, we refer to the collection [rhoXY*] as the genome signature. We establish that the differences between [rhoXY*] vectors of 50-kb sample contigs of different genomes virtually always exceed the differences between those of the same genomes. Various di- and tetranucleotide biases are identified. In particular, we find that the dinucleotide CpG=CG is underrepresented in many thermophiles (e.g., M. jannaschii, Sulfolobus sp., and M. thermoautotrophicum) but overrepresented in halobacteria. TA is broadly underrepresented in prokaryotes and eukaryotes, but normal counts appear in Sulfolobus and P. aerophilum sequences. More than for any other bacterial genome, palindromic tetranucleotides are underrepresented in H. influenzae. The M. jannaschii sequence is unprecedented in its extreme underrepresentation of CTAG tetranucleotides and in the anomalous distribution of CTAG sites around the genome. Comparative analysis of numbers of long tetranucleotide microsatellites distinguishes H. influenzae. Dinucleotide relative abundance differences between bacterial sequences are compared. For example, in these assessments of differences, the cyanobacteria Synechocystis, Synechococcus, and Anabaena do not form a coherent group and are as far from each other as general gram-negative sequences are from general gram-positive sequences. The difference of M. jannaschii from low-G+C gram-positive proteobacteria is one-half of the difference from gram-negative proteobacteria. Interpretations and hypotheses center on the role of the genome signature in highlighting similarities and dissimilarities across different classes of prokaryotic species, possible mechanisms underlying the genome signature, the form and level of genome compositional flux, the use of the genome signature as a chronometer of molecular phylogeny, and implications with respect to the three putative eubacterial, archaeal, and eukaryote domains of life and to the origin and early evolution of eukaryotes.
机译:我们比较并对比了跨越15种具有大量基因组序列集合的原核生物的全基因组组成偏差和短寡核苷酸的分布。这些包括七个完整的基因组(大肠杆菌,流感嗜血杆菌,生殖器支原体,肺炎支原体,肺炎链球菌属菌株PCC6803,詹氏甲烷球菌和嗜热热单生菌)。关键观察结果涉及同一基因组内多个50 kb不交叠重叠群上二核苷酸相对丰度分布图的恒定性。 (对于所有XY而言,特征谱均为rhoXY * = fXY * / fX * fY *,其中fX *表示核苷酸X的频率,fY *表示二核苷酸XY的频率,两者均由与其反向互补序列连接的序列计算得出。)基于这种恒定性,我们将集合[rhoXY *]称为基因组签名。我们确定,不同基因组的50kb样品重叠群的[rhoXY *]向量之间的差异实际上总是超过相同基因组之间的差异。鉴定了各种二核苷酸和四核苷酸偏差。特别地,我们发现二核苷酸CpG = CG在许多嗜热菌中(例如,詹氏甲烷球菌,Sulfolobus sp。和嗜热自养球菌)的代表性不足,但在卤代细菌中的代表性较高。 TA在原核生物和真核生物中的代表性不足,但是正常计数出现在Sulfolobus和P. aerophilum序列中。在流感嗜血杆菌中,回文四核苷酸比其他任何细菌基因组都多。詹氏甲烷八叠球菌序列在CTAG四核苷酸的极度代表性不足以及基因组周围CTAG位点的异常分布方面是空前的。长四核苷酸微卫星数目的比较分析可区分流感嗜血杆菌。比较细菌序列之间的二核苷酸相对丰度差异。例如,在这些差异评估中,蓝细菌集胞藻,集球菌和鱼腥藻不形成连贯的基团,并且彼此之间距离较远,因为一般革兰氏阴性序列来自一般革兰氏阳性序列。詹氏支原体与低G + C革兰氏阳性菌的区别是与革兰氏阴性菌的区别的一半。解释和假设集中于基因组签名在强调不同类别的原核生物之间的相似性和异同性,基因组签名潜在的潜在机制,基因组组成通量的形式和水平,将基因组签名用作分子计时表方面的作用。系统发育,以及对生命的三个假定的真细菌,古细菌和真核生物领域以及真核生物的起源和早期进化的启示。

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