Jiang Jingchen, Zhao Liuya, Yan Lan, Zhang Lulu, Cao Yingying, Wang Yan, Jiang Yuanying, Yan Tianhua, Cao Yongbing
Department of Pharmacology; School of Pharmacy; China Pharmaceutical University; Nanjing, PR China.
R & D Center of New Drug; School of Pharmacy; Second Military Medical University; Shanghai, PR China.
Virulence. 2014 Feb 15;5(2):245-52. doi: 10.4161/viru.27278. Epub 2013 Dec 6.
A number of abundant mobile genetic elements called retrotransposons reverse transcribe RNA to generate DNA for insertion into eukaryotic genomes. Non-long-terminal repeat (non-LTR) retrotransposons represent a major class of retrotransposons, and transposons that move by target-primed reverse transcription lack LTRs characteristic of retroviruses and retroviral-like transposons. Yeast model systems in Candida albicans and Saccharomyces cerevisiae have been developed for the study of non-LTR retrotransposons. Non-LTR retrotransposons are divided into LINEs (long interspersed nuclear elements), SINEs (short interspersed nuclear elements), and SVA (SINE, VNTR, and Alu). LINE-1 elements have been described in fungi, and several families called Zorro elements have been detected from C. albicans. They are all members of L1 clades. Through a mechanism named target-primed reverse transcription (TPRT), LINEs translocate the new copy into the target site to initiate DNA synthesis primed by the 3' OH of the broken strand. In this article, we describe some advances in the research on structural features and origin of non-LTR retrotransposons in C. albicans, and discuss mechanisms underlying their reverse transcription and integration of the donor copy into the target site.
许多丰富的移动遗传元件,即逆转录转座子,通过逆转录RNA来生成DNA,以便插入真核生物基因组。非长末端重复(non-LTR)逆转录转座子是逆转录转座子的主要类别,通过靶标引发的逆转录进行移动的转座子缺乏逆转录病毒和类逆转录病毒转座子特有的长末端重复序列。白色念珠菌和酿酒酵母中的酵母模型系统已被开发用于研究非LTR逆转录转座子。非LTR逆转录转座子分为长散在核元件(LINEs)、短散在核元件(SINEs)和SVA(SINE、可变数目串联重复序列和Alu)。LINE-1元件已在真菌中被描述,并且从白色念珠菌中检测到了几个名为佐罗元件的家族。它们都是L1进化枝的成员。通过一种名为靶标引发的逆转录(TPRT)的机制,LINEs将新拷贝转移到靶位点,以由断裂链的3' OH引发DNA合成。在本文中,我们描述了白色念珠菌中非LTR逆转录转座子的结构特征和起源研究的一些进展,并讨论了它们逆转录以及供体拷贝整合到靶位点的潜在机制。