Self-assembly of RNF126 into inactive homodimers releases functionally active forms of RNF8 in respo

来源 :The 16th Ataxia-Telangiectasia Workshop (ATW-2015)6th Intern | 被引量 : 0次 | 上传用户:zhouyiai1015
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
Cells have evolved sophisticated mechanisms to maintain genomic integrity in response to DNA damage.As important as is activation of DNA damage signaling cascades, negative regulation of DNA damage response (DDR) is also crucial for preventing unintended cellular consequences.Here, we identified RNF 126 as a novel negative regulator of the DDR.
其他文献
Chemotherapeutic and radiation treatments cause a variety of genotoxic insults that lead to cell death in rapidly proliferating cancer cells.To survive genotoxic insults,cancer cells depend on multipl
会议
Glioblastoma multiforme (GBM) is one of the most frequent and lethal cancers.However, the molecular events and their interplay underlying carcinogenesis remain elusive.
会议
The maintenance of genome integrity is important in all cells.To conserve genome integrity, cells developed multiple molecular pathways to repair damaged DNA.Proliferating Cell Nuclear Antigen (PCNA),
会议
Ataxia-telangiectasia (AT) is an inherited autosomal recessive disorder caused by mutations in the ATM (ataxia-telangiectasia mutated) gene.In spite of progressive neurological dysfunction, especially
We report the case of a 6-year-old girl with Ataxia Telangiectasia who developed a left cerebellar astrocytoma and a contralateral cerebellar infarction, the latter never reported in AT patients.
Poly (ADP-ribose) polymerase-1 (PARP-1) serves as a critical enzyme in the repair of single-strand DNA breaks.PARP inhibitors (PARPi) can sensitize tumors to DNA-damaging agents and to selectively kil
Introduction: Ataxia-telangiectasia (A-T) is a rare genetic disease caused by mutations in the ataxia telangiectasia mutated (ATM) gene that codifies for a protein kinase belonging to the PI3-kinase f
Ataxia-telangiectasia (A-T) is an autosomal recessive disease caused by mutations in the ATM gene.A-T patients are characterised by increased cancer development,radiosensitivity, immunodeficiency and
Introduction: Ataxia Telangiectasia (A-T) is a rare genetic disorder with symptoms including ataxia and involuntary movements, higher risk of infections, and high risk of cancer [1].There is currently
Exposure to environmental pollutants, pesticides, or radiation inflicts oxidative DNA damage to the genome, which underlies the pathogenesis of many diseases.DNA double strand breaks (DSBs) are a freq
会议