'''Caenorhabditis elegans''' (
IPA: ) is a free-living
nematode (roundworm), about 1
mm in length, which lives in temperate soil environments. Research into the
molecular and
developmental biology of ''C. elegans'' was begun in
1974 by
Sydney Brenner [1] and it has since been used extensively as a
model organism.
Biology
''C. elegans'' is unsegmented,
vermiform,
bilaterally symmetrical, with a
cuticle integument, four main epidermal cords and a fluid-filled
pseudocoelomate cavity. Members of the species have many of the same organ systems as other animals. In the wild, they feed on bacteria that develop on decaying vegetable matter. ''C. elegans'' has both a
hermaphrodite sex, and a very rare male population, which makes up 0.05% of the total ''C. elegans'' on average. The basic anatomy of ''C. elegans'' includes a mouth, pharynx, intestine,
gonad, and collagenous cuticle. Males have a single-lobed gonad,
vas deferens, and a tail specialized for mating. Hermaphrodites have two ovaries, oviducts, spermatheca, and a single uterus.
''C. elegans'' eggs are laid by the hermaphrodite. After hatching, they pass through four
larval stages (L1-L4). When crowded or in the absence of food, ''C. elegans'' can enter an alternative third larval stage called the
dauer state. Dauer larvae are stress-resistant and do not age. Hermaphrodites produce all their sperm in the L4 stage (150 sperm per gonadal arm) and then switch over to producing oocytes. The sperm are stored in the same area of the gonad as the oocytes until the first oocyte pushes the sperm into the spermatheca (a kind of chamber where the oocytes become fertilized by the sperm).
[2]. The male can inseminate the hermaphrodite, which will use male sperm preferentially (both types of sperm are stored in the spermatheca). When self-inseminated the wild-type worm will lay approximately 300 eggs. When inseminated by a male, the number of progeny can exceed 1,000. At 20
°C, the laboratory strain of ''C. elegans'' has an average life span of approximately 2–3 weeks and a generation time of approximately 4 days. Hermaphrodites can mate with males or self-fertilize.
''C. elegans'' has five pairs of
autosomes and one pair of
sex chromosomes. Sex in ''C. elegans'' is based on an
X0 sex-determination system. Hermaphrodite ''C. elegans'' have a matched pair of sex chromosomes (XX); the rare males have only one sex chromosome (X0).
Laboratory uses
''C. elegans'' is studied as a
model organism for a variety of reasons.
Strains are cheap to breed and can be frozen. When subsequently thawed they remain viable, allowing long-term storage. Because the complete cell lineage of the species has been determined, ''C. elegans'' has proven especially useful for studying
cellular differentiation.
From a research perspective, ''C. elegans'' has the advantage of being a
multicellular eukaryotic organism which is simple enough to be studied in great detail. The developmental fate of every single
somatic cell (959 in the adult hermaphrodite; 1031 in the adult male) has been mapped out. These patterns of cell lineage are largely invariant between individuals, in contrast to mammals where cell development from the embryo is more largely dependent on cellular cues. In both sexes, a large number of additional cells (131 in the hermaphrodite, most of which would otherwise become
neurons), are eliminated by programmed cell death (
apoptosis).

Wild-type ''C. elegans'' hermaphrodite stained to highlight the nuclei of all cells
In addition, ''C. elegans'' is one of the simplest organisms with a
nervous system. In the hermaphrodite, this comprises 302
neurons whose pattern of connectivity has been completely mapped out, and shown to be a
small-world network [3]. Research has explored the neural mechanisms responsible for several of the more interesting behaviors shown by ''C. elegans'', including
chemotaxis,
thermotaxis,
mechanotransduction, and male mating behavior. Interestingly, the neurons fire no
action potentials.
A useful feature of ''C. elegans'' is that it is relatively straightforward to disrupt the function of specific genes by
RNA interference (RNAi).
Silencing the function a gene in this way can sometimes allow a researcher to infer what the function of that gene may be. The nematode can either be soaked in (or injected with) a solution of double stranded
RNA, the sequence of which is complentary to the sequence of the gene that the researcher wishes to disable. Alternatively, worms can be fed on genetically transformed
bacteria which
express the double stranded RNA of interest.
C. elegans has also been useful in the study of
meiosis. As sperm and egg nuclei move down the length of the gonad, they undergo a temporal progression through meiotic events. This progression means that every nuclei at a given position in the gonad will be at roughly the same step in meiosis, eliminating the difficulties of heterogeneous populations of cells.
The organism has also been identified as a model for
nicotine dependence as it has been found to experience the same symptoms humans experience when they
quit smoking.
[4]
As for most model organisms, there is a dedicated online database for the species that is actively curated by scientists working in this field. The
WormBase database attempts to collate all published information on ''C. elegans'' and other related nematodes. A reward of $4000 has been advertised on their website, for the finder of a new species of closely related nematode.
[5] Such a discovery would broaden research opportunities with the worm.
[6]
The Genome
''C. elegans'' was the first multicellular organism to have its
genome completely
sequenced. The finished genome sequence was published in 1998,
[7] although a number of small gaps were present (the last gap was finished by October 2002). The ''C. elegans'' genome sequence is approximately 100 million
base pairs long and contains approximately 20,000
genes. The vast majority of these genes encode for
proteins but there are likely to be as many as 1,000
RNA genes. Scientific curators continue to appraise the set of known genes, such that new gene predictions continue to be added and incorrect ones modified or removed.
In 2003, the genome sequence of the related nematode ''
C. briggsae'' was also determined, allowing researchers to study the comparative genomics of these two organisms
[8]. Work is now ongoing to determine the genome sequences of more nematodes from the same
genus such as ''C. remanei''
[1], ''C. japonica''
[2] and ''C. brenneri''
[3]. These newer genome sequences are being determined by using the
whole genome shotgun technique which means that the resulting genome sequences are likely to not be as complete or accurate as ''C. elegans'' (which was sequenced using the 'hierarchical' or
clone-by-clone appoach).
The official version of the ''C. elegans'' genome sequence continues to change as and when new evidence reveals errors in the original sequencing (
DNA sequencing is not an error free process). Most changes are usually minor, adding or removing only a few
base pairs (bp) of DNA.
E.g. the WS169 release of
WormBase (December 2006) lists a net gain of 6 bp to the genome sequence
[ WormBaseWiki WS169 release notes ]. Occasionally more extensive changes are made, e.g. the WS159 release of May 2006 added over 300 bp to the sequence
[ WormBaseWiki WS159 release notes ].
Nematode evolution
It has been shown that a small number of conserved
protein sequences from
sponges are more similar to humans than to ''C. elegans''
[9]. This suggests that there has been an accelerated rate of evolution in the ''C. elegans''
lineage. The same study found that several
phylogenetically ancient genes are not present in ''C. elegans''.
''C. elegans'' scientists''
In 2002, the
Nobel Prize for Medicine was awarded to
Sydney Brenner,
H. Robert Horvitz and
John Sulston for their work on the genetics of organ development and
programmed cell death (PCD) in ''C. elegans''. The 2006
Nobel Prize in Physiology or Medicine was awarded to
Andrew Fire and
Craig C. Mello, for their discovery of
RNA interference in ''C. elegans''.
[10]
Because all research into ''C. elegans'' essentially started with
Sydney Brenner in the 1970's, many scientists working in this field share a close connection to Brenner (they either worked as a
post-doctoral or
post-graduate researcher in Brenner's lab or in the lab of someone who previously worked with Brenner). Because most people who worked in his lab went on to establish their own worm research labs, there is now a fairly well documented 'lineage' of ''C. elegans'' scientists. This lineage was recorded in some detail at the 2003 International Worm Meeting and the results were stored in the
Wormbase database.
''C. elegans'' in the media
''C. elegans'' made news when it was discovered that specimens had survived the
Space Shuttle ''Columbia'' disaster in February 2003.
[11]
See also
★
Animal testing on invertebrates
References
1. The Genetics of ''Caenorhabditis elegans'', Brenner, S., , , Genetics, 1974
2. ''fog-2'' and the Evolution of Self-Fertile Hermaphroditism in ''Caenorhabditis'', Nayak, S., J. Goree & T. Schedl, , , PLoS Biology, 2004
3. Collective dynamics of 'small-world' networks, Watts D. J. & S. H. Strogatz, , , Nature, 1998
4. A C. elegans Model of Nicotine-Dependent Behavior: Regulation by TRP-Family Channels, Feng et al., , , Cell, 2006
5. ''Caenorhabditis'' isolation guide
6. Slime for a dime, , , , Science, 2007
7. Genome sequence of the nematode ''C. elegans'': a platform for investigating biology, The ''C. elegans'' Sequencing Consortium, , , Science, 1998
8. The Genome Sequence of ''Caenorhabditis briggsae'': A Platform for Comparative Genomics, Stein, L. D. ''et al.'', , , PLoS Biology, 2003
9. Sponge proteins are more similar to those of ''Homo sapiens'' than to ''Caenorhabditis elegans'', , V, Gamulin, Biological Journal of the Linnean Society,
10. A. Fire, S.Q. Xu, M.K. Montgomery, S.A. Kostas, S. E. Driver, C.C. Mello: ''Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans.'' In: ''Nature.'' 391/1998, S. 806-811,
11. Worms survived Columbia disaster
Relevant publications
★
The Structure of Nematodes, Bird, A. F & J. Bird, , , Academic Press, Inc., San Diego, 1991,
★ Gamulin, Vera; Müller, Isabel M. & Müller, Werner E. G. (2000): Sponge proteins are more similar to those of ''Homo sapiens'' than to ''Caenorhabditis elegans''. ''
Biol. J. Linn. Soc.'' '71'(4): 821–828.
HTML abstract
★
''C. elegans'': A practical approach, Hope, I. A., , , Oxford University Press, New York, 1999,
★
''C. elegans'' II, Riddle, D.L., T. Blumenthal, R. J. Meyer & J. R. Priess, , , Cold Spring Harbor Laboratory Press, New York, 1997,
Online resources
★
WormBase - an extensive online database covering the biology and genomics of ''C. elegans'' and other nematodes
★
WormBook - a free online compendium of all aspects of ''C. elegans'' biology, including laboratory protocols
★
Wormatlas - an online database for behavioral and structural anatomy of ''C. elegans''
★
Wellcome Trust Sanger Institute ''C. elegans'' page - half of the genome sequence is still maintained by this institute
★
WashU Genome Sequencing Center ''C. elegans'' page - the institute maintaining the other half of the genome
★
AceView WormGenes - another genome database for ''C. elegans'', maintained at the NCBI
★
Worm Classroom - An education portal for ''C. elegans''
★
Textpresso - WormBase search engine
★
''C. elegans'' movies - Timelapse films made by ''C. elegans'' researchers worldwide
★
''C. elegans'' II - a free online textbook.
★
Silencing Genomes RNA interference (RNAi) experiments and bioinformatics in ''C. elegans'' for education. From the Dolan DNA Learning Center of Cold Spring Harbor Laboratory.
Nobel lectures
★ Brenner S (2002) Nature's Gift to Science. In. http://nobelprize.org/nobel_prizes/medicine/laureates/2002/brenner-lecture.pdf
★ Horvitz HR (2002) Worms, Life and Death. In. http://nobelprize.org/nobel_prizes/medicine/laureates/2002/horvitz-lecture.pdf
★ Sulston JE (2002) The Cell Lineage and Beyond. In. http://nobelprize.org/nobel_prizes/medicine/laureates/2002/sulston-lecture.pdf
External links
★
Nematodes With a Craving for Nicotine