Visualizing plant development and gene expression in three dimensions using optical projection tomography

被引:110
作者
Lee, Karen
Avondo, Jerome
Morrison, Harris
Blot, Lilian
Stark, Margaret
Sharpe, James
Bangham, Andrew
Coen, Enrico
机构
[1] John Innes Inst, Dept Cell & Dev Biol, Norwich NR4 7UH, Norfolk, England
[2] Univ E Anglia, Sch Comp Sci, Norwich NR4 7TJ, Norfolk, England
[3] Western Gen Hosp, Opt Project Tomog Grp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[4] Western Gen Hosp, Edinburgh Mouse Atlas Grp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
D O I
10.1105/tpc.106.043042
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
A deeper understanding of the mechanisms that underlie plant growth and development requires quantitative data on three-dimensional ( 3D) morphology and gene activity at a variety of stages and scales. To address this, we have explored the use of optical projection tomography ( OPT) as a method for capturing 3D data from plant specimens. We show that OPT can be conveniently applied to a wide variety of plant material at a range of scales, including seedlings, leaves, flowers, roots, seeds, embryos, and meristems. At the highest resolution, large individual cells can be seen in the context of the surrounding plant structure. For naturally semitransparent structures, such as roots, live 3D imaging using OPT is also possible. 3D domains of gene expression can be visualized using either marker genes, such as beta-glucuronidase, or more directly by whole-mount in situ hybridization. We also describe tools and software that allow the 3D data to be readily quantified and visualized interactively in different ways.
引用
收藏
页码:2145 / 2156
页数:12
相关论文
共 51 条
[11]   In vivo analysis of cell division, cell growth, and differentiation at the shoot apical meristem in arabidopsis [J].
Grandjean, O ;
Vernoux, T ;
Laufs, P ;
Belcram, K ;
Mizukami, Y ;
Traas, J .
PLANT CELL, 2004, 16 (01) :74-87
[12]   In vivo anterior segment imaging in the rat eye with high speed white light full-field optical coherence tomography [J].
Grieve, K ;
Dubois, A ;
Simonutti, M ;
Paques, M ;
Sahel, J ;
Le Gargasson, JF ;
Boccara, C .
OPTICS EXPRESS, 2005, 13 (16) :6286-6295
[13]   Nonlinear structured-illumination microscopy: Wide-field fluorescence imaging with theoretically unlimited resolution [J].
Gustafsson, MGL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (37) :13081-13086
[14]   Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly [J].
Haseloff, J ;
Siemering, KR ;
Prasher, DC ;
Hodge, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2122-2127
[15]   Patterns of auxin transport and gene expression during primordium development revealed by live imaging of the Arabidopsis inflorescence meristem [J].
Heisler, MG ;
Ohno, C ;
Das, P ;
Sieber, P ;
Reddy, GV ;
Long, JA ;
Meyerowitz, EM .
CURRENT BIOLOGY, 2005, 15 (21) :1899-1911
[16]   Optical coherence microscopy.: A technology for rapid, in vivo, non-destructive visualization of plants and plant cells1[w] [J].
Hettinger, JW ;
Mattozzi, MDP ;
Myers, WR ;
Williams, ME ;
Reeves, A ;
Parsons, RL ;
Haskell, RC ;
Petersen, DC ;
Wang, RY ;
Medford, JI .
PLANT PHYSIOLOGY, 2000, 123 (01) :3-15
[17]   In vivo observation of cavitation and embolism repair using magnetic resonance imaging [J].
Holbrook, NM ;
Ahrens, ET ;
Burns, MJ ;
Zwieniecki, MA .
PLANT PHYSIOLOGY, 2001, 126 (01) :27-31
[18]   Optical sectioning deep inside live embryos by selective plane illumination microscopy [J].
Huisken, J ;
Swoger, J ;
Del Bene, F ;
Wittbrodt, J ;
Stelzer, EHK .
SCIENCE, 2004, 305 (5686) :1007-1009
[19]  
Jain AK., 1989, Fundamentals of Digital Image Processing
[20]  
Jefferson R A, 1987, EMBO J, V6, P3901