Replication of simple DNA repeats

描述（由申请人提供）：简单DNA重复序列的扩增与人类近30种遗传性疾病有关。这项建议集中在负责重复扩增的分子机制。在先前的资助期间，我们发现复制叉在哺乳动物细胞中的可扩展重复序列处停滞。导致复制抑制的重复序列的长度与其在人类谱系中扩展的阈值长度非常匹配。我们进一步研究了酵母中重复序列介导的复制阻断的控制，发现叉稳定蛋白Tof 1和Mrc 1通过可扩展的重复序列促进复制。最重要的是，我们已经开发了一个新的实验系统来分析大规模的重复扩增酵母。该系统的独特优势在于，它使我们能够监测携带者大小重复序列在疾病大小范围内的扩展。扩增速率大大提高后，失活的复制叉稳定剂，TOF 1，而显着减少，在缺乏的DNA解旋酶SGS 1或复制后修复调节Rad 6。总之，这些数据涉及DNA复制和/或复制后修复重复不稳定性，我们将进一步评估这一假设在酵母和哺乳动物细胞中的建议。我们将研究各种三，四和五核苷酸重复在我们的酵母实验系统中的大规模扩增，通过分析重复扩增的速率和可视化的复制叉进展通过各种重复。扩展重复序列抑制酵母中的基因表达，就像它们在人类疾病中所做的那样。因此，我们将通过研究各种重复序列对转录、RNA剪接和RNA稳定性的影响来分析我们系统中基因阻遏的机制。对于转录时不稳定的重复序列，我们将为它们的大规模扩增开发一个不同的系统，使它们定位在非转录区。为了深入了解重复不稳定性的遗传控制，我们将分析我们大量的突变体中的重复扩增和收缩，这些突变体影响酵母中的DNA复制、修复和重组。我们将进一步进行酵母突变体的遗传筛选，这些突变体显示出使用诱变酵母基因组文库的基因破坏增加的大规模重复扩增率或减少的重复收缩率。在哺乳动物细胞中，我们将使用复制中间体的二维电泳来评估pSV 2neo附加体中各种可扩展重复序列的复制。我们还将研究可扩展重复序列是否触发附加型脆性。这些基因的哺乳动物同源物的表达，来自酵母筛选，将被siRNA敲低，以研究它们在重复介导的复制阻断和脆性中的作用。最后，我们将尝试开发一种新的系统，用于监测大规模的重复扩增人类细胞中使用一个专门设计的HyTK选择盒结合的翻转整合方法。这项提案的长期目标是了解负责人类重复扩张和收缩的分子机制。 公共卫生相关性：超过20种人类遗传性疾病是由人类基因内简单DNA重复的不可控制的扩张引起的。它们包括使人衰弱的神经系统疾病，如亨廷顿氏病、脆性X染色体智力低下、强直性肌营养不良等。这项提议旨在解开造成这一现象的分子机制。

DESCRIPTION (provided by applicant): Expansions of simple DNA repeats are implicated in nearly thirty hereditary disorders in humans. This proposal concentrates on molecular mechanisms responsible for repeat expansions. During the previously funded period we have found that replication forks stalled at expandable repeats in mammalian cells. The length of the repeat, which caused replication inhibition, closely matched the threshold length for its expansion in human pedigrees. We have further studied the control of repeat-mediated replication blockage in yeast to discover that the fork stabilizing proteins, Tof1 and Mrc1, facilitated replication through expandable repeats. Most significantly, we have developed a new experimental system to analyze large-scale repeat expansions in yeast. The unique advantage of this system is that it allowed us to monitor expansions of the carrier-size repeats well into the disease-size range. Expansion rates were strongly elevated upon inactivation of the replication fork stabilizer, Tof1, while significantly decreased in the lack of the DNA helicase Sgs1 or the post-replicative repair regulator Rad6. Altogether these data implicate DNA replication and/or post-replicative repair in repeat instability; we will further assess this hypothesis in yeast and mammalian cells in this proposal. We will study large-scale expansions of various tri-, tetra-and pentanucleotide repeats in our yeast experimental system by analyzing the rates of repeat expansions and visualizing the replication fork progression through various repeats. Expanded repeats inhibited gene expression in yeast as they do in human diseases. We will, therefore, analyze the mechanisms responsible for gene repression in our system by studying the effects of various repeats on transcription, RNA splicing and RNA stability. For repeats that are unstable when transcribed, we will develop a different system for their large-scale expansions, so that they are positioned in a non- transcribed area. To get insight into the genetic control of repeat instability, we will analyze repeat expansions and contractions in our large collection of mutants affecting DNA replication, repair and recombination in yeast. We will further perform genetic screens for yeast mutants that show either an increased rate of large-scale repeat expansions or a decreased rate of repeat contractions using gene disruption with a mutagenized yeast genomic library. In mammalian cells, we will evaluate replication of various expandable repeats in the pSV2neo episome using two-dimensional electrophoresis of replication intermediates. We will also study whether expandable repeats trigger episomal fragility. Expression of mammalian homologues of the genes, which came up from the yeast screens, will be knocked down by siRNAs to study their role in repeat-mediated replication blockage and fragility. Finally, we will attempt to develop a new system for monitoring large-scale repeat expansions in human cells using a specifically designed HyTK selectable cassette combined with the Flip-In integration approach. The long-term goal of this proposal is to understand molecular mechanisms responsible for repeat expansions and contractions in humans. PUBLIC HEALTH RELEVANCE: More than two dozen human hereditary diseases are caused by uncontrollable expansions of simple DNA repetitions within human genes. They include debilitating neurological disorders, such as Huntington's disease, fragile X mental retardation, myotonic dystrophy and others. This proposal is to unravel molecular mechanisms responsible for this phenomenon.