Genetic Information Research Institute, Mountain View, CA, USA.
Mob DNA. 2010 Jan 25;1(1):3. doi: 10.1186/1759-8753-1-3.
In eukaryotes, long terminal repeat (LTR) retrotransposons such as Copia, BEL and Gypsy integrate their DNA copies into the host genome using a particular type of DDE transposase called integrase (INT). The Gypsy INT-like transposase is also conserved in the Polinton/Maverick self-synthesizing DNA transposons and in the 'cut and paste' DNA transposons known as TDD-4 and TDD-5. Moreover, it is known that INT is similar to bacterial transposases that belong to the IS3, IS481, IS30 and IS630 families. It has been suggested that LTR retrotransposons evolved from a non-LTR retrotransposon fused with a DNA transposon in early eukaryotes. In this paper we analyze a diverse superfamily of eukaryotic cut and paste DNA transposons coding for INT-like transposase and discuss their evolutionary relationship to LTR retrotransposons.
A new diverse eukaryotic superfamily of DNA transposons, named Ginger (for 'Gypsy INteGrasE Related') DNA transposons is defined and analyzed. Analogously to the IS3 and IS481 bacterial transposons, the Ginger termini resemble those of the Gypsy LTR retrotransposons. Currently, Ginger transposons can be divided into two distinct groups named Ginger1 and Ginger2/Tdd. Elements from the Ginger1 group are characterized by approximately 40 to 270 base pair (bp) terminal inverted repeats (TIRs), and are flanked by CCGG-specific or CCGT-specific target site duplication (TSD) sequences. The Ginger1-encoded transposases contain an approximate 400 amino acid N-terminal portion sharing high amino acid identity to the entire Gypsy-encoded integrases, including the YPYY motif, zinc finger, DDE domain, and, importantly, the GPY/F motif, a hallmark of Gypsy and endogenous retrovirus (ERV) integrases. Ginger1 transposases also contain additional C-terminal domains: ovarian tumor (OTU)-like protease domain or Ulp1 protease domain. In vertebrate genomes, at least two host genes, which were previously thought to be derived from the Gypsy integrases, apparently have evolved from the Ginger1 transposase genes. We also introduce a second Ginger group, designated Ginger2/Tdd, which includes the previously reported DNA transposon TDD-4.
The Ginger superfamily represents eukaryotic DNA transposons closely related to LTR retrotransposons. Ginger elements provide new insights into the evolution of transposable elements and certain transposable element (TE)-derived genes.
在真核生物中,长末端重复(LTR)反转录转座子,如 Copia、BEL 和 Gypsy,利用一种称为整合酶(INT)的特殊 DDE 转座酶将其 DNA 拷贝整合到宿主基因组中。Gypsy INT 样转座酶也在 Polinton/Maverick 自合成 DNA 转座子和称为 TDD-4 和 TDD-5 的“切和粘贴”DNA 转座子中保守。此外,已知 INT 与属于 IS3、IS481、IS30 和 IS630 家族的细菌转座酶相似。有人提出,LTR 反转录转座子是从早期真核生物中融合了 DNA 转座子的非 LTR 反转录转座子进化而来的。在本文中,我们分析了一类多样化的真核“切和粘贴”DNA 转座子超家族,这些超家族编码 INT 样转座酶,并讨论了它们与 LTR 反转录转座子的进化关系。
定义并分析了一类新的多样化的真核“切和粘贴”DNA 转座子超家族,命名为 Ginger(意为“Gypsy INteGrasE Related”)DNA 转座子。类似于 IS3 和 IS481 细菌转座酶,Ginger 末端类似于 Gypsy LTR 反转录转座子的末端。目前,Ginger 转座子可分为两个不同的组,分别命名为 Ginger1 和 Ginger2/Tdd。Ginger1 组的元件特征是大约 40 到 270 个碱基对(bp)的末端反向重复(TIR),两侧是 CCGG 特异性或 CCGT 特异性靶序列重复(TSD)序列。Ginger1 编码的转座酶包含约 400 个氨基酸的 N 端部分,与整个 Gypsy 编码的整合酶具有高度的氨基酸同一性,包括 YPYY 基序、锌指、DDE 结构域,以及重要的 GPY/F 基序,这是 Gypsy 和内源性逆转录病毒(ERV)整合酶的标志。Ginger1 转座酶还包含其他 C 端结构域:卵巢肿瘤(OTU)样蛋白酶结构域或 Ulp1 蛋白酶结构域。在脊椎动物基因组中,至少有两个先前被认为来自 Gypsy 整合酶的宿主基因,显然是从 Ginger1 转座酶基因进化而来的。我们还引入了第二个 Ginger 组,称为 Ginger2/Tdd,其中包括先前报道的 DNA 转座子 TDD-4。
Ginger 超家族代表与 LTR 反转录转座子密切相关的真核 DNA 转座子。Ginger 元件为转座元件和某些转座元件(TE)衍生基因的进化提供了新的见解。