Fundación Instituto de Estudios Avanzados and United Nations University UNU-BIOLAC, Caracas, Venezuela.
Front Cell Infect Microbiol. 2020 Jan 10;9:439. doi: 10.3389/fcimb.2019.00439. eCollection 2019.
Like in most eukaryotes, the linear chromosomes of end in a nucleoprotein structure called the telomere, which is preceded by regions of variable length called subtelomeres. Together telomeres and subtelomeres are dynamic sites where DNA sequence rearrangements can occur without compromising essential interstitial genes or chromosomal synteny. Good examples of subtelomeres involvement are the expansion of human olfactory receptors genes, variant surface antigens in , and mating types. telomeres are made of long stretches of the hexameric repeat 5'-TTAGGG-OH-3', and its subtelomeres are enriched in genes and pseudogenes from the large gene families RHS, TS and DGF1, DEAD/H-RNA helicase and N-acetyltransferase, intermingled with sequences of retrotransposons elements. In particular, members of the Trans-sialidase type II family appear to have played a role in shaping the current telomere structure. Although the structure and function of telomeric and subtelomeric regions have been documented, recent experiments are providing new insights into 's telomere-subtelomere dynamics. In this review, I discuss the co-evolution of telomere, subtelomeres and the TS gene family, and the role that these regions may have played in shaping 's genome.
与大多数真核生物一样, 的线性染色体以一种称为端粒的核蛋白结构结束,端粒之前是长度可变的称为端粒区的区域。端粒和端粒区共同构成了动态位点,在这些位点上,DNA 序列重排可以发生,而不会危及间质基因或染色体的同线性。端粒区参与的一个很好的例子是人类嗅觉受体基因的扩展、 的变体表面抗原和 的交配型。端粒由六聚体重复 5'-TTAGGG-OH-3'的长链组成,其端粒区富含来自 RHS、TS 和 DGF1、DEAD/H-RNA 解旋酶和 N-乙酰转移酶等大型基因家族的基因和假基因,与逆转座子元件的序列交织在一起。特别是,转涎酶 II 型家族的成员似乎在塑造当前 的端粒结构方面发挥了作用。尽管已经记录了 的端粒和端粒区的结构和功能,但最近的实验为 的端粒-端粒区动力学提供了新的见解。在这篇综述中,我讨论了端粒、端粒区和 TS 基因家族的共同进化,以及这些区域在塑造 的基因组中可能发挥的作用。