Measurement of replication structures at the nanometer scale using super-resolution light microscopy

被引:80
作者
Baddeley, D. [2 ]
Chagin, V. O. [1 ,3 ]
Schermelleh, L. [4 ]
Martin, S. [5 ]
Pombo, A. [5 ]
Carlton, P. M. [6 ]
Gahl, A. [4 ,7 ]
Domaing, P. [7 ]
Birk, U. [2 ]
Leonhardt, H. [4 ]
Cremer, C. [2 ,8 ,9 ]
Cardoso, M. C. [1 ,7 ]
机构
[1] Tech Univ Darmstadt, Dept Biol, Darmstadt, Germany
[2] Univ Heidelberg, Kirchhoff Inst Phys, D-6900 Heidelberg, Germany
[3] Russian Acad Sci, Inst Cytol, St Petersburg 194064, Russia
[4] Univ Munich, Ctr Integrated Prot Sci, Dept Biol 2, Munich, Germany
[5] Univ London Imperial Coll Sci Technol & Med, Fac Med, MRC, Ctr Clin Sci, London SW7 2AZ, England
[6] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[7] Max Delbruck Ctr Mol Med, Berlin, Germany
[8] Univ Heidelberg, Inst Pharm & Mol Biol, D-6900 Heidelberg, Germany
[9] Jackson Lab, Inst Mol Biophys, Bar Harbor, ME USA
基金
英国医学研究理事会;
关键词
MODULATED ILLUMINATION MICROSCOPY; DNA-REPLICATION; S-PHASE; NUCLEAR-ORGANIZATION; CHROMOSOME STRUCTURE; SMI MICROSCOPY; CELL-NUCLEI; DYNAMICS; SITES; SIZE;
D O I
10.1093/nar/gkp901
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA replication, similar to other cellular processes, occurs within dynamic macromolecular structures. Any comprehensive understanding ultimately requires quantitative data to establish and test models of genome duplication. We used two different super-resolution light microscopy techniques to directly measure and compare the size and numbers of replication foci in mammalian cells. This analysis showed that replication foci vary in size from 210 nm down to 40 nm. Remarkably, spatially modulated illumination (SMI) and 3D-structured illumination microscopy (3D-SIM) both showed an average size of 125 nm that was conserved throughout S-phase and independent of the labeling method, suggesting a basic unit of genome duplication. Interestingly, the improved optical 3D resolution identified 3- to 5-fold more distinct replication foci than previously reported. These results show that optical nanoscopy techniques enable accurate measurements of cellular structures at a level previously achieved only by electron microscopy and highlight the possibility of high-throughput, multispectral 3D analyses.
引用
收藏
页码:e8.1 / e8.11
页数:11
相关论文
共 33 条
[1]   DNA DOUBLE LABELING WITH IDURD AND CLDURD FOR SPATIAL AND TEMPORAL ANALYSIS OF CELL-PROLIFERATION AND DNA-REPLICATION [J].
ATEN, JA ;
BAKKER, PJM ;
STAP, J ;
BOSCHMAN, GA ;
VEENHOF, CHN .
HISTOCHEMICAL JOURNAL, 1992, 24 (05) :251-259
[2]   Nanostructure analysis using spatially modulated illumination microscopy [J].
Baddeley, David ;
Batram, Claudia ;
Weiland, Yanina ;
Cremer, Christoph ;
Birk, Udo J. .
NATURE PROTOCOLS, 2007, 2 (10) :2640-2646
[3]   High precision size measurement of centromere 8 and the 8q24/c-myc gene region in metaphase and interphase human fibroblasts indicate differential condensation [J].
Batram, C. ;
Baddeley, D. ;
Kreth, G. ;
Cremer, C. .
JOURNAL OF STRUCTURAL BIOLOGY, 2008, 164 (03) :293-303
[4]  
BRANCO MR, 2006, METHODS EXPRESS SERI, P201
[5]  
Failla A. V., 2003, ComPlexUs, V1, P77, DOI 10.1159/000070464
[6]   Nanosizing of fluorescent objects by spatially modulated illumination microscopy [J].
Failla, AV ;
Spoeri, U ;
Albrecht, B ;
Kroll, A ;
Cremer, C .
APPLIED OPTICS, 2002, 41 (34) :7275-7283
[7]   Subwavelength size determination by spatially modulated illumination virtual microscopy [J].
Failla, AV ;
Cavallo, A ;
Cremer, C .
APPLIED OPTICS, 2002, 41 (31) :6651-6659
[8]   Visualizing the dynamics of chromosome structure formation coupled with DNA replication [J].
Gotoh, Eisuke .
CHROMOSOMA, 2007, 116 (05) :453-462
[9]   Fixation-induced redistribution of hyperphosphorylated RNA polymerase II in the nucleus of human cells [J].
Guillot, PV ;
Xie, SQ ;
Hollinshead, M ;
Pombo, A .
EXPERIMENTAL CELL RESEARCH, 2004, 295 (02) :460-468
[10]   Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination [J].
Gustafsson, Mats G. L. ;
Shao, Lin ;
Carlton, Peter M. ;
Wang, C. J. Rachel ;
Golubovskaya, Inna N. ;
Cande, W. Zacheus ;
Agard, David A. ;
Sedat, John W. .
BIOPHYSICAL JOURNAL, 2008, 94 (12) :4957-4970