• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation.人近端 Xp 区的 FoSTeS、MMBIR 和 NAHR 以及人类 Xq 等臂染色体形成的机制。
Hum Mol Genet. 2011 May 15;20(10):1925-36. doi: 10.1093/hmg/ddr074. Epub 2011 Feb 24.
2
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.微同源介导机制是导致 FOXL2 基因或其调控域非重复致病微缺失的基础。
PLoS Genet. 2013;9(3):e1003358. doi: 10.1371/journal.pgen.1003358. Epub 2013 Mar 14.
3
The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.DNA复制的FoSTeS/MMBIR机制可在人类中产生基因组、基因和外显子的复杂重排。
Nat Genet. 2009 Jul;41(7):849-53. doi: 10.1038/ng.399. Epub 2009 Jun 21.
4
Mechanisms of structural chromosomal rearrangement formation.结构性染色体重排形成的机制。
Mol Cytogenet. 2022 Jun 14;15(1):23. doi: 10.1186/s13039-022-00600-6.
5
Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosis.原发性骨髓纤维化中LCR介导的17号等臂染色体常见重排的间期荧光原位杂交筛查
Am J Hematol. 2005 Aug;79(4):309-13. doi: 10.1002/ajh.20366.
6
Decoding NF1 Intragenic Copy-Number Variations.解读神经纤维瘤病1型基因内拷贝数变异
Am J Hum Genet. 2015 Aug 6;97(2):238-49. doi: 10.1016/j.ajhg.2015.06.002. Epub 2015 Jul 16.
7
Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene.神经纤维瘤病1型(NF1)基因内由回文序列介导且依赖复制的致病性结构重排。
Hum Mutat. 2014 Jul;35(7):891-8. doi: 10.1002/humu.22569. Epub 2014 May 21.
8
Aberrant X chromosomal rearrangement through multi-step template switching during sister chromatid formation in a patient with severe hemophilia A.在一名严重血友病 A 患者的姐妹染色单体形成过程中,通过多步模板转换出现异常的 X 染色体重排。
Mol Genet Genomic Med. 2020 Sep;8(9):e1390. doi: 10.1002/mgg3.1390. Epub 2020 Jul 5.
9
A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders.一种用于产生与基因组疾病相关的非重复性重排的DNA复制机制。
Cell. 2007 Dec 28;131(7):1235-47. doi: 10.1016/j.cell.2007.11.037.
10
Inheritance of Charcot-Marie-Tooth disease 1A with rare nonrecurrent genomic rearrangement.遗传性腓骨肌萎缩症 1A 伴罕见非重复基因组重排。
Neurogenetics. 2011 Feb;12(1):51-8. doi: 10.1007/s10048-010-0272-3. Epub 2010 Dec 31.

引用本文的文献

1
Chromoanasynthesis.染色体组分析
Methods Mol Biol. 2025;2968:35-51. doi: 10.1007/978-1-0716-4750-9_2.
2
Microsatellite break-induced replication generates highly mutagenized extrachromosomal circular DNAs.微卫星断裂诱导复制产生高度诱变的染色体外环状DNA。
NAR Cancer. 2024 Jun 8;6(2):zcae027. doi: 10.1093/narcan/zcae027. eCollection 2024 Jun.
3
SETD2 safeguards the genome against isochromosome formation.SETD2 可保护基因组免受等臂染色体形成的影响。
Proc Natl Acad Sci U S A. 2023 Sep 26;120(39):e2303752120. doi: 10.1073/pnas.2303752120. Epub 2023 Sep 18.
4
Suppressors of Break-Induced Replication in Human Cells.抑制人细胞中的断裂诱导复制。
Genes (Basel). 2023 Feb 3;14(2):398. doi: 10.3390/genes14020398.
5
Fine Breakpoint Mapping by Genome Sequencing Reveals the First Large X Inversion Disrupting the Gene in a Patient with Syndromic Cataracts.全基因组测序精确定位断点揭示首例大型 X 染色体倒位导致综合征性白内障患者 基因失活
Int J Mol Sci. 2021 Nov 24;22(23):12713. doi: 10.3390/ijms222312713.
6
Replication stress at microsatellites causes DNA double-strand breaks and break-induced replication.微卫星处的复制压力导致 DNA 双链断裂和断裂诱导复制。
J Biol Chem. 2020 Nov 6;295(45):15378-15397. doi: 10.1074/jbc.RA120.013495. Epub 2020 Sep 1.
7
Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence.阳性性染色体非整倍体无创产前筛查结果后的诊断细胞遗传学检测:5 例病例报告及证据的系统回顾。
Mol Genet Genomic Med. 2020 Jul;8(7):e1297. doi: 10.1002/mgg3.1297. Epub 2020 May 8.
8
Transcriptional silencing of centromere repeats by heterochromatin safeguards chromosome integrity.异染色质对着丝粒重复序列的转录沉默可保护染色体的完整性。
Curr Genet. 2019 Oct;65(5):1089-1098. doi: 10.1007/s00294-019-00975-x. Epub 2019 Apr 17.
9
The dark side of centromeres: types, causes and consequences of structural abnormalities implicating centromeric DNA.着丝粒的阴暗面:涉及着丝粒 DNA 的结构异常的类型、原因和后果。
Nat Commun. 2018 Oct 18;9(1):4340. doi: 10.1038/s41467-018-06545-y.
10
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.神经发育障碍中的反复性新生突变:特征及临床意义。
Genome Med. 2017 Nov 27;9(1):101. doi: 10.1186/s13073-017-0498-x.

本文引用的文献

1
Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.Xp11.2 内的大反向重复序列存在于 Turner 综合征等臂 X 染色体的断裂点处。
Hum Mol Genet. 2010 Sep 1;19(17):3383-93. doi: 10.1093/hmg/ddq250. Epub 2010 Jun 22.
2
Genomic rearrangements in inherited disease and cancer.遗传性疾病和癌症中的基因组重排。
Semin Cancer Biol. 2010 Aug;20(4):222-33. doi: 10.1016/j.semcancer.2010.05.007. Epub 2010 Jun 9.
3
Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability.与 CMT1A 或 HNPP 相关的非重现性基因组重排机制:罕见的 CNVs 是遗传缺失的原因。
Am J Hum Genet. 2010 Jun 11;86(6):892-903. doi: 10.1016/j.ajhg.2010.05.001. Epub 2010 May 20.
4
Molecular and evolutionary characteristics of the fraction of human alpha satellite DNA associated with CENP-A at the centromeres of chromosomes 1, 5, 19, and 21.与染色体 1、5、19 和 21 着丝粒处的 CENP-A 相关的人α卫星 DNA 片段的分子和进化特征。
BMC Genomics. 2010 Mar 23;11:195. doi: 10.1186/1471-2164-11-195.
5
Widespread gene conversion in centromere cores.着丝粒核心内广泛的基因转换。
PLoS Biol. 2010 Mar 9;8(3):e1000327. doi: 10.1371/journal.pbio.1000327.
6
Centromeres convert but don't cross.着丝粒转换但不交叉。
PLoS Biol. 2010 Mar 9;8(3):e1000326. doi: 10.1371/journal.pbio.1000326.
7
Nearby inverted repeats fuse to generate acentric and dicentric palindromic chromosomes by a replication template exchange mechanism.附近的反向重复序列通过复制模板交换机制融合,产生无着丝粒和双着丝粒的回文染色体。
Genes Dev. 2009 Dec 15;23(24):2876-86. doi: 10.1101/gad.1863009.
8
Fusion of nearby inverted repeats by a replication-based mechanism leads to formation of dicentric and acentric chromosomes that cause genome instability in budding yeast.通过基于复制的机制使附近的反向重复序列融合,会导致双着丝粒染色体和无着丝粒染色体的形成,从而在芽殖酵母中引起基因组不稳定。
Genes Dev. 2009 Dec 15;23(24):2861-75. doi: 10.1101/gad.1862709.
9
Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes.等臂双着丝粒Y染色体和性疾病是维持回文序列的同源重组的副产物。
Cell. 2009 Sep 4;138(5):855-69. doi: 10.1016/j.cell.2009.07.042.
10
Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females.复杂节段性重复介导了一种复发性的X染色体重复dup(X)(p11.22-p11.23),该重复与男性和女性的智力发育迟缓、语言发育迟缓以及脑电图异常有关。
Am J Hum Genet. 2009 Sep;85(3):394-400. doi: 10.1016/j.ajhg.2009.08.001. Epub 2009 Aug 27.

人近端 Xp 区的 FoSTeS、MMBIR 和 NAHR 以及人类 Xq 等臂染色体形成的机制。

FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation.

机构信息

Department of Medical Genetics, University Medical Center Utrecht, Universiteitsweg 100, 3584 CG Utrecht, The Netherlands.

出版信息

Hum Mol Genet. 2011 May 15;20(10):1925-36. doi: 10.1093/hmg/ddr074. Epub 2011 Feb 24.

DOI:10.1093/hmg/ddr074
PMID:21349920
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3428953/
Abstract

The recently described DNA replication-based mechanisms of fork stalling and template switching (FoSTeS) and microhomology-mediated break-induced replication (MMBIR) were previously shown to catalyze complex exonic, genic and genomic rearrangements. By analyzing a large number of isochromosomes of the long arm of chromosome X (i(Xq)), using whole-genome tiling path array comparative genomic hybridization (aCGH), ultra-high resolution targeted aCGH and sequencing, we provide evidence that the FoSTeS and MMBIR mechanisms can generate large-scale gross chromosomal rearrangements leading to the deletion and duplication of entire chromosome arms, thus suggesting an important role for DNA replication-based mechanisms in both the development of genomic disorders and cancer. Furthermore, we elucidate the mechanisms of dicentric i(Xq) (idic(Xq)) formation and show that most idic(Xq) chromosomes result from non-allelic homologous recombination between palindromic low copy repeats and highly homologous palindromic LINE elements. We also show that non-recurrent-breakpoint idic(Xq) chromosomes have microhomology-associated breakpoint junctions and are likely catalyzed by microhomology-mediated replication-dependent recombination mechanisms such as FoSTeS and MMBIR. Finally, we stress the role of the proximal Xp region as a chromosomal rearrangement hotspot.

摘要

最近描述的基于 DNA 复制的叉停顿和模板转换(FoSTeS)和微同源介导的断裂诱导复制(MMBIR)机制先前被证明可以催化复杂的外显子、基因和基因组重排。通过使用全基因组平铺路径阵列比较基因组杂交(aCGH)、超高分辨率靶向 aCGH 和测序分析大量 X 染色体长臂等臂染色体(i(Xq)),我们提供了证据表明 FoSTeS 和 MMBIR 机制可以产生大规模的染色体结构重排,导致整个染色体臂的缺失和重复,从而表明 DNA 复制机制在基因组疾病和癌症的发展中起着重要作用。此外,我们阐明了双着丝粒 i(Xq)(idic(Xq))形成的机制,并表明大多数 idic(Xq) 染色体是由回文低拷贝重复序列和高度同源回文 LINE 元件之间的非等位基因同源重组产生的。我们还表明,非重现性断裂点 idic(Xq) 染色体具有微同源相关的断裂点连接,并且可能由 FoSTeS 和 MMBIR 等微同源介导的复制依赖性重组机制催化。最后,我们强调了近端 Xp 区域作为染色体重排热点的作用。