Modern mosaic analysis in the zebrafish

被引:47
作者
Carmany-Rampey, Amanda
Moens, Cecilia B.
机构
[1] Fred Hutchinson Canc Res Ctr, HHMI, Seattle, WA 98115 USA
[2] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98115 USA
关键词
zebrafish; mosaic analysis; genetic mosaic transplantation;
D O I
10.1016/j.ymeth.2006.02.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
One of the most powerful tools used to gain insight into complex developmental processes is the analysis of mosaic embryos. A mosaic is defined as an organism that contains cells of more than one genotype, usually wild-type and mutant. It is the interplay between wildtype and mutant cells in the mosaic that reveals information about the normal function of the mutated gene. Mosaic analysis has been utilized extensively in Caenorhabditis elegans, Drosophila, mice, and zebrafish to elucidate when, where, and how a gene acts during development. In the zebrafish, mosaic analysis has been used to dissect a number of different developmental processes, including gastrulation movements, mesoderm and endoderm specification, neuronal patterning and migration, axon pathfinding, angiogenesis, and cardiac, retinal, and neural crest development. Mosaic analysis is a particularly effective method for understanding gene function in the zebrafish, a model organism particularly suited to forward genetic, molecular, and classical embryological approaches. These attributes, when combined with the accessibility and optical clarity of the zebrafish embryo, facilitate the real time observation of individual cell behaviors and interactions within mosaic embryos. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:228 / 238
页数:11
相关论文
共 52 条
  • [1] Embryonic precursor cells from the rhombic lip are specified to a cerebellar granule neuron identity
    Alder, J
    Cho, NK
    Hatten, ME
    [J]. NEURON, 1996, 17 (03) : 389 - 399
  • [2] Genetic mosaic techniques for studying Drosophila development
    Blair, SS
    [J]. DEVELOPMENT, 2003, 130 (21): : 5065 - 5072
  • [3] Transition from non-motile behaviour to directed migration during early PGC development in zebrafish
    Blaser, H
    Eisenbeiss, S
    Neuman, M
    Reichman-Fried, M
    Thisse, B
    Thisse, C
    Raz, E
    [J]. JOURNAL OF CELL SCIENCE, 2005, 118 (17) : 4027 - 4038
  • [4] Single-cell internalization during zebrafish gastrulation
    Carmany-Rampey, A
    Schier, AF
    [J]. CURRENT BIOLOGY, 2001, 11 (16) : 1261 - 1265
  • [5] The zebrafish Nodal signal Squint functions as a morphogen
    Chen, Y
    Schier, AF
    [J]. NATURE, 2001, 411 (6837) : 607 - 610
  • [6] Production of maternal-zygotic mutant zebrafish by germ-line replacement
    Ciruna, B
    Weidinger, G
    Knaut, H
    Thisse, B
    Thisse, C
    Raz, E
    Schier, AF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (23) : 14919 - 14924
  • [7] EDhA4 is required for cell adhesion and rhombomere-boundary formation in the zebrafish
    Cooke, JE
    Kemp, HA
    Moens, CB
    [J]. CURRENT BIOLOGY, 2005, 15 (06) : 536 - 542
  • [8] Zebrafish foggy/spt5 is required for migration of facial branchiomotor neurons but not for their survival
    Cooper, KL
    Armstrong, J
    Moens, CB
    [J]. DEVELOPMENTAL DYNAMICS, 2005, 234 (03) : 651 - 658
  • [9] Autonomous and nonautonomous functions for Hox/Pbx in branchiomotor neuron development
    Cooper, KL
    Leisenring, WM
    Moens, CB
    [J]. DEVELOPMENTAL BIOLOGY, 2003, 253 (02) : 200 - 213
  • [10] Cornell RA, 2002, DEVELOPMENT, V129, P2639