Georgiev G P
Eur J Biochem. 1984 Dec 3;145(2):203-20. doi: 10.1111/j.1432-1033.1984.tb08541.x.
Mobile genetic elements were discovered by McClintock while analysing unstable mutations in maize. The structural and functional studies of such elements became possible after their cloning, first from the genome of Drosophila melanogaster. In particular, Ilyin et al. demonstrated the varying location of the described elements in D. melanogaster chromosomes, thus providing the first evidence of their mobility. Mobile elements comprise a significant part of the genetic material in D. melanogaster (not less than 10%). Several classes of mobile elements do exist. Mobile dispersed genetic elements (mdg elements) are among the best characterized ones. Mdg elements are represented in the genome by dozens of families, each consisting of 10-150 copies. They are very similar structurally to proviruses of endogenous retroviruses. In particular, the both contain long terminal repeats (LTRs). The nucleotide sequences of LTRs and their flanking sequences of several mdg elements were determined. Their analysis suggested that RNA reverse transcription should be involved in the mdg amplification. It has been found that putative transposition intermediates, i.e. extrachromosomal DNA copies of mdg elements, are synthesized by reverse transcriptase in D. melanogaster culture cells. Another type of mobile genes is represented by P factor and similar elements. P factor seems to encode 'transposase' participating in direct excision and insertion of P elements themselves as well as of other mobile genes (mdg and fold-back elements). Besides these 'active transposons' which encode the enzyme machinery for transposition, a number of other sequences which may be transposed are present in the genome. RNAs synthesized on such elements can serve as a template for reverse transcriptase, and the DNA formed can then be inserted at new sites of the genome. Among such sequences are the so-called short ubiquitous repeats: B1 and B2 in mouse genome and Alu in human genome. We found that, at least in several cases, B-type sequences were located at the 3' end of mRNA. Short repetitive sequences were also detected at the 3' end of certain mRNAs of D. melanogaster. Usually the transpositions of mobile genes occur very rarely. However, under certain conditions, for example, in hybrid dysgenesis, they become more frequent. The strain with a mutation in cut locus was obtained in hybrid dysgenesis. This mutation depends on an insertion of mdg4 at the cut locus. Genetic instability in this strain is maintained for a long time. 'Transposition bursts' were found to occur in some germ cells.(ABSTRACT TRUNCATED AT 400 WORDS)
移动遗传元件是麦克林托克在分析玉米的不稳定突变时发现的。在这类元件被克隆后,对其进行结构和功能研究成为可能,最初是从黑腹果蝇的基因组中克隆出来的。特别是,伊林等人证明了所描述的元件在黑腹果蝇染色体中的位置各不相同,从而提供了它们具有移动性的首个证据。移动元件构成了黑腹果蝇遗传物质的重要部分(不少于10%)。确实存在几类移动元件。移动分散遗传元件(mdg元件)是特征最为明确的元件之一。mdg元件在基因组中由几十个家族代表,每个家族由10 - 150个拷贝组成。它们在结构上与内源性逆转录病毒的前病毒非常相似。特别是,两者都包含长末端重复序列(LTRs)。测定了几种mdg元件的LTRs及其侧翼序列的核苷酸序列。对它们的分析表明,RNA逆转录应该参与mdg的扩增。已经发现,假定的转座中间体,即mdg元件的染色体外DNA拷贝,是由黑腹果蝇培养细胞中的逆转录酶合成的。另一类移动基因由P因子及类似元件代表。P因子似乎编码“转座酶”,参与P元件自身以及其他移动基因(mdg和回折元件)的直接切除和插入。除了这些编码转座酶机制的“活性转座子”外,基因组中还存在许多可能被转座的其他序列。在这类元件上合成的RNA可以作为逆转录酶的模板,然后形成的DNA可以插入到基因组的新位点。这类序列中有所谓的短遍在重复序列:小鼠基因组中的B1和B2以及人类基因组中的Alu。我们发现,至少在几种情况下,B型序列位于mRNA的3'端。在黑腹果蝇的某些mRNA的3'端也检测到了短重复序列。通常移动基因的转座非常罕见。然而,在某些条件下,例如在杂种不育中,它们会变得更加频繁。在杂种不育中获得了在cut位点发生突变的菌株。这种突变取决于mdg4在cut位点的插入。该菌株的遗传不稳定性会长期维持。在一些生殖细胞中发现了“转座爆发”。