Lampson B C, Inouye S, Inouye M
Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854.
Prog Nucleic Acid Res Mol Biol. 1991;40:1-24. doi: 10.1016/s0079-6603(08)60838-7.
The msDNA-retron element represents the first prokaryotic member of the large and diverse retroelement family found in many eukaryotic genomes (Table II). This prokaryotic retroelement exists as a single copy element in the chromosome of two different bacterial groups: the common soil microbe M. xanthus and the enteric bacterium E. coli. It encodes an RT similar to the polymerases found in retroviruses, containing most of the strictly conserved amino acids found in all RTs. The RT is responsible for the production of an unusual extrachromosomal RNA-DNA molecule known as msDNA. Each composed of a short single strand of RNA and a short single strand of DNA, msDNAs vary considerably in their primary nucleotide sequences, but all share certain secondary structural features, including the unique 2',5' branch linkage that joins the 5' end of the DNA chain to the 2' position of an internal guanosine residue of the RNA strand. It is proposed that msDNA is synthesized by reverse transcription of a precursor RNA transcribed from a region of the retron containing the genes msr (encoding the RNA portion) and msd (encoding the DNA portion) and the ORF (encoding the RT). The precursor RNA transcript folds into a stable secondary structure that serves as both the primer and the template for the synthesis of msDNA. The msDNA-retron elements of E. coli are found in less than 10% of all strains observed, are heterogeneous in nature, and have an atypical aminoacid codon usage for this species, suggesting that this element was transmitted to E. coli by some other source. The presence of directly repeated 26-base-pair sequences flanking the junctions of the Ec67-retron of E. coli also suggests that it may be a mobile element. However, the msDNA-retrons of M. xanthus appear to be as old as other genes native to this species, based on codon-usage data for the RT genes and the fact that every strain of M. xanthus appears to have the same type of msDNA. If the msDNA-retron element originated with the myxobacteria, it would place the existence of retrons before the appearance of eukaryotic cells, suggesting that the bacterial element is perhaps the ancestral gene from which eukaryotic retroviruses and other retroelements evolved.(ABSTRACT TRUNCATED AT 400 WORDS)
msDNA-反转录子元件是在许多真核生物基因组中发现的庞大而多样的反转录元件家族中的首个原核生物成员(表二)。这种原核生物反转录元件以单拷贝元件的形式存在于两种不同细菌群体的染色体中:常见的土壤微生物黄色粘球菌和肠道细菌大肠杆菌。它编码一种与逆转录病毒中发现的聚合酶相似的逆转录酶,包含所有逆转录酶中发现的大部分严格保守的氨基酸。该逆转录酶负责产生一种不寻常的染色体外RNA-DNA分子,称为msDNA。msDNA由一条短的单链RNA和一条短的单链DNA组成,其一级核苷酸序列差异很大,但都具有某些二级结构特征,包括独特的2',5'分支连接,该连接将DNA链的5'末端连接到RNA链内部鸟苷残基的2'位置。有人提出,msDNA是由从包含msr基因(编码RNA部分)、msd基因(编码DNA部分)和开放阅读框(编码逆转录酶)的反转录子区域转录的前体RNA逆转录合成的。前体RNA转录本折叠成稳定的二级结构,作为msDNA合成的引物和模板。在所有观察到的大肠杆菌菌株中,不到10%含有大肠杆菌的msDNA-反转录子元件,其性质具有异质性,并且该物种的氨基酸密码子使用情况不典型,这表明该元件是由其他某种来源传递给大肠杆菌的。大肠杆菌Ec67-反转录子连接处两侧存在直接重复的26个碱基对序列,这也表明它可能是一种可移动元件。然而,基于逆转录酶基因的密码子使用数据以及黄色粘球菌的每个菌株似乎都具有相同类型的msDNA这一事实,黄色粘球菌的msDNA-反转录子似乎与该物种的其他原生基因一样古老。如果msDNA-反转录子元件起源于粘细菌,那么反转录子的存在将早于真核细胞的出现,这表明细菌元件可能是真核逆转录病毒和其他反转录元件进化而来的祖先基因。(摘要截短至400字)