Blackburn E, Bhattacharyya A, Gilley D, Kirk K, Krauskopf A, McEachern M, Prescott J, Ware T
Department of Microbiology and Immunology, University of California, San Francisco 94143-0414, USA.
Ciba Found Symp. 1997;211:2-13; discussion 15-9. doi: 10.1002/9780470515433.ch2.
The tandemly repeated DNA sequence of telomeres is typically specified by the ribonucleoprotein enzyme telomerase. Telomerase copies part of its intrinsic RNA moiety to make one strand of the telomeric repeat DNA. Recent work has led to the concept of a telomere homeostasis system. We have been studying two key physical components of this system: the telomere itself and telomerase. Mutating the template sequence of telomerase RNA caused various phenotypes: (1) mutating specific residues in the ciliate Tetrahymena and two yeasts showed that they are required for critical aspects of telomerase action; (2) certain mutated telomeric sequences caused a previously unreported phenotype, i.e. a strong anaphase block in Tetrahymena micronuclei; and (3) certain template mutations in the telomerase RNA gene of the yeast Kluyveromyces lactis led to unregulated telomere elongation, which in some cases was directly related to loss of binding to K. lactis Rap1p. Using K. lactis carrying alterations in the genes for Rap1p and other silencing components, we proposed a general model for telomere length homeostasis: namely, that the structure and DNA length of the DNA-protein complex that comprises the telomere are key determinants of telomerase access, and hence the frequency of action of telomerase, at the telomere.
端粒的串联重复DNA序列通常由核糖核蛋白酶端粒酶决定。端粒酶复制其自身RNA部分的一部分,以形成端粒重复DNA的一条链。最近的研究产生了端粒稳态系统的概念。我们一直在研究该系统的两个关键物理成分:端粒本身和端粒酶。突变端粒酶RNA的模板序列会导致各种表型:(1)在纤毛虫四膜虫和两种酵母中突变特定残基表明,它们是端粒酶作用关键方面所必需的;(2)某些突变的端粒序列导致了一种以前未报道的表型,即在四膜虫微核中出现强烈的后期阻断;(3)乳酸克鲁维酵母端粒酶RNA基因中的某些模板突变导致端粒不受调控地延长,在某些情况下,这与失去与乳酸克鲁维酵母Rap1p的结合直接相关。利用在Rap1p和其他沉默成分基因中携带改变的乳酸克鲁维酵母,我们提出了一个端粒长度稳态的通用模型:即,构成端粒的DNA-蛋白质复合物的结构和DNA长度是端粒酶在端粒处的可及性以及端粒酶作用频率的关键决定因素。