Bouallègue Maryem, Rouault Jacques-Deric, Hua-Van Aurélie, Makni Mohamed, Capy Pierre
Laboratoire Evolution, Génomes, Comportement, Ecologie CNRS, Univ. Paris-Sud, IRD, Université Paris-Saclay, Gif-sur-Yvette, France.
Université de Tunis El Manar, Faculté des Sciences de Tunis, UR11ES10 Génomique des Insectes Ravageurs de Cultures, Tunis, Tunisie.
Genome Biol Evol. 2017 Feb 1;9(2):323-339. doi: 10.1093/gbe/evw292.
The piggyBac transposable element was originally isolated from the cabbage looper moth, Trichoplusia ni, in the 1980s. Despite its early discovery and specificity compared to the other Class II elements, the diversity and evolution of this superfamily have been only partially analyzed. Two main types of elements can be distinguished: the piggyBac-like elements (PBLE) with terminal inverted repeats, untranslated region, and an open reading frame encoding a transposase, and the piggyBac-derived sequences (PGBD), containing a sequence derived from a piggyBac transposase, and which correspond to domesticated elements. To define the distribution, their structural diversity and phylogenetic relationships, analyses were conducted using known PBLE and PGBD sequences to scan databases. From this data mining, numerous new sequences were characterized (50 for PBLE and 396 for PGBD). Structural analyses suggest that four groups of PBLE can be defined according to the presence/absence of sub-terminal repeats. The transposase is characterized by highly variable catalytic domain and C-terminal region. There is no relationship between the structural groups and the phylogeny of these PBLE elements. The PGBD are clearly structured into nine main groups. A new group of domesticated elements is suspected in Neopterygii and the remaining eight previously described elements have been investigated in more detail. In all cases, these sequences are no longer transposable elements, the catalytic domain of the ancestral transposase is not always conserved, but they are under strong purifying selection. The phylogeny of both PBLE and PGBD suggests multiple and independent domestication events of PGBD from different PBLE ancestors.
猪gyBac转座元件最初于20世纪80年代从甘蓝尺蛾(Trichoplusia ni)中分离出来。尽管与其他II类元件相比它发现较早且具有特异性,但该超家族的多样性和进化仅得到了部分分析。可区分出两种主要类型的元件:具有末端反向重复序列、非翻译区和编码转座酶的开放阅读框的猪gyBac样元件(PBLE),以及包含源自猪gyBac转座酶的序列且对应于驯化元件的猪gyBac衍生序列(PGBD)。为了确定它们的分布、结构多样性和系统发育关系,利用已知的PBLE和PGBD序列对数据库进行扫描分析。通过这种数据挖掘,鉴定出了许多新序列(PBLE为50个,PGBD为396个)。结构分析表明,根据亚末端重复序列的有无可将PBLE分为四组。转座酶的特征是催化结构域和C末端区域高度可变。这些PBLE元件的结构组与系统发育之间没有关系。PGBD明显分为九个主要组。在新翅类动物中怀疑存在一组新的驯化元件,并且对其余八个先前描述的元件进行了更详细的研究。在所有情况下,这些序列不再是转座元件,祖先转座酶的催化结构域并不总是保守的,但它们受到强烈的纯化选择。PBLE和PGBD的系统发育表明,PGBD从不同的PBLE祖先发生了多次独立的驯化事件。