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Tetrahymena Pot2 Is a Developmentally Regulated Paralog of Pot1 That Localizes to Chromosome Breakage Sites but Not to Telomeres

机译:四膜虫Pot2是Pot1的发育受调控的旁系同源物,其定位于染色体断裂位点而不是端粒

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Tetrahymena telomeres are protected by a protein complex composed of Pot1, Tpt1, Pat1, and Pat2. Pot1 binds the 3′ overhang and serves multiple roles in telomere maintenance. Here we describe Pot2, a paralog of Pot1 which has evolved a novel function during Tetrahymena sexual reproduction. Pot2 is unnecessary for telomere maintenance during vegetative growth, as the telomere structure is unaffected by POT2 macronuclear gene disruption. Pot2 is expressed only in mated cells, where it accumulates in developing macronuclei around the time of two chromosome processing events: internal eliminated sequence (IES) excision and chromosome breakage. Chromatin immunoprecipitation (ChIP) demonstrated Pot2 localization to regions of chromosome breakage but not to telomeres or IESs. Pot2 association with chromosome breakage sites (CBSs) occurs slightly before chromosome breakage. Pot2 did not bind CBSs or telomeric DNA in vitro, suggesting that it is recruited to CBSs by another factor. The telomere proteins Pot1, Pat1, and Tpt1 and the IES binding factor Pdd1 fail to colocalize with Pot2. Thus, Pot2 is the first protein found to associate specifically with CBSs. The selective association of Pot2 versus Pdd1 with CBSs or IESs indicates a mechanistic difference between the chromosome processing events at these two sites. Moreover, ChIP revealed that histone marks characteristic of IES processing, H3K9me3 and H3K27me3, are absent from CBSs. Thus, the mechanisms of chromosome breakage and IES excision must be fundamentally different. Our results lead to a model where Pot2 directs chromosome breakage by recruiting telomerase and/or the endonuclease responsible for DNA cleavage to CBSs.
机译:四膜虫端粒受到由Pot1,Tpt1,Pat1和Pat2组成的蛋白质复合物的保护。 Pot1结合3'突出端,并在端粒维持中发挥多种作用。在这里,我们描述Pot2,Pot1的旁系同源物,它在四膜虫有性生殖过程中进化了一种新功能。由于端粒结构不受 POT2 大核基因破坏的影响,Pot2对于营养生长期间的端粒维护是不必要的。 Pot2仅在交配的细胞中表达,在两个染色体处理事件(内部消除序列(IES)切除和染色体断裂)的时间里,它在发育中的大核中积累。染色质免疫沉淀(ChIP)证明Pot2定位在染色体断裂区域,而不是端粒或IESs。 Pot2与染色体断裂位点(CBS)的关联发生在染色体断裂之前。 Pot2在体外不结合CBS或端粒DNA,这表明它是由另一种因子募集到CBS的。端粒蛋白Pot1,Pat1,Tpt1和IES结合因子Pdd1无法与Pot2共定位。因此,Pot2是第一个与CBS特异性结合的蛋白质。 Pot2与Pdd1与CBS或IES的选择性关联表明在这两个位点的染色体加工事件之间存在机械差异。此外,ChIP揭示了CBS中没有IES处理的组蛋白标记H3K9me3和H3K27me3。因此,染色体断裂和IES切除的机制必须根本不同。我们的结果导致了一个模型,其中Pot2通过募集负责DNA裂解为CBS的端粒酶和/或核酸内切酶来指导染色体断裂。

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