Basic Caenorhabditis elegans Methods: Synchronization and Observation

被引:339
作者
Porta-de-la-Riva, Montserrat [1 ,2 ]
Fontrodona, Laura [1 ]
Villanueva, Alberto [1 ,2 ]
Ceron, Julian [1 ,2 ]
机构
[1] Bellvitge Inst Biomed Res, Dept Canc & Human Mol Genet, Barcelona, Spain
[2] Bellvitge Inst Biomed Res, C Elegans Core Facil, Barcelona, Spain
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2012年 / 64期
关键词
Basic Protocols; Issue; 64; Genetics; Developmental Biology; Molecular Biology; C; elegans; synchronization; development; Nomarski; DAPI staining;
D O I
10.3791/4019
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Research into the molecular and developmental biology of the nematode Caenorhabditis elegans was begun in the early seventies by Sydney Brenner and it has since been used extensively as a model organism (1). C. elegans possesses key attributes such as simplicity, transparency and short life cycle that have made it a suitable experimental system for fundamental biological studies for many years (2). Discoveries in this nematode have broad implications because many cellular and molecular processes that control animal development are evolutionary conserved (3). C. elegans life cycle goes through an embryonic stage and four larval stages before animals reach adulthood. Development can take 2 to 4 days depending on the temperature. In each of the stages several characteristic traits can be observed. The knowledge of its complete cell lineage (4,5) together with the deep annotation of its genome turn this nematode into a great model in fields as diverse as the neurobiology (6), aging (7,8), stem cell biology (9) and germ line biology (10). An additional feature that makes C. elegans an attractive model to work with is the possibility of obtaining populations of worms synchronized at a specific stage through a relatively easy protocol. The ease of maintaining and propagating this nematode added to the possibility of synchronization provide a powerful tool to obtain large amounts of worms, which can be used for a wide variety of small or high-throughput experiments such as RNAi screens, microarrays, massive sequencing, immunoblot or in situ hybridization, among others. Because of its transparency, C. elegans structures can be distinguished under the microscope using Differential Interference Contrast microscopy, also known as Nomarski microscopy. The use of a fluorescent DNA binder, DAPI (4', 6-diamidino-2-phenylindole), for instance, can lead to the specific identification and localization of individual cells, as well as subcellular structures/defects associated to them.
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页数:9
相关论文
共 19 条
[1]   MECHANISM OF PARALYSING ACTION OF TETRAMISOLE ON ASCARIS SOMATIC MUSCLE [J].
ACEVES, J ;
ERLIJ, D ;
MARTINEZ.R .
BRITISH JOURNAL OF PHARMACOLOGY, 1970, 38 (03) :602-+
[2]  
[Anonymous], 1988, NEMATODE CAENORHABDI
[3]  
BRENNER S, 1974, GENETICS, V77, P71
[4]  
Depuydt G, 2010, ADV EXP MED BIOL, V694, P81
[5]  
Garigan D, 2002, GENETICS, V161, P1101
[6]  
Hobert Oliver, 2010, WormBook, P1, DOI 10.1895/wormbook.1.12.2
[7]  
Jia KL, 2010, ADV EXP MED BIOL, V694, P47
[8]   Caenorhabditis elegans as a Model for Stem Cell Biology [J].
Joshi, Pradeep M. ;
Riddle, Misty R. ;
Djabrayan, Nareg J. V. ;
Rothman, Joel H. .
DEVELOPMENTAL DYNAMICS, 2010, 239 (05) :1539-1554
[9]   POST-EMBRYONIC CELL LINEAGES OF THE HERMAPHRODITE AND MALE GONADS IN CAENORHABDITIS-ELEGANS [J].
KIMBLE, J ;
HIRSH, D .
DEVELOPMENTAL BIOLOGY, 1979, 70 (02) :396-417
[10]   The threshold for polyglutamine-expansion protein aggregation and cellular toxicity is dynamic and influenced by aging in Caenorhabditis elegans [J].
Morley, JF ;
Brignull, HR ;
Weyers, JJ ;
Morimoto, RI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10417-10422