Summary of Features

Additional Non-Mammalian Model Organisms (Continued)
February 1999

 

S. purpuratus
(Purple Sea Urchin)

A. california
(Aplysia)

Genome

haploid chromosome #

42

17

Size

800 Mb

1,000 Mb

fraction sequenced

~3%

225 cDNAs; only 125 in DB

genes/ORFs

cDNA/EST sequence

~2,500

 

   

Characteristics

   

cellular organization

deuterostome metazoan; indirect development with pelagic feeding larva; metamorphosing after 5 weeks; embryogenesis complete at 1800-cell stage in 3 days

multicellular; map cell-cell connections easily->cell bodies are peripherally located and accessible for injection and other mainpulations

Ploidy

diploid

some very large neurons are up to 7,000 x haploid genome=15 duplications

generation time

~1 year

4 months to 6 months

(egg->egg)

   

Cultivation

egg to egg culture, including large scale embryo, larva and adult maintenance easily performed

 

 

 

 

Transfection/transgenic

injection of expression vectors into eggs very efficient

transfection: yes, by microinjection; in princiiple: any gene into any cell; transgenic: no

gene inactivation

TKO, other methods

by injection of antisense RNAs or oligonucleotides

   

Mutants

several naturally occurring under study

no

   

Cell Culture

 

yes, primary only

   

Storage

   

gametes

several weeks

no

embryos

 

no

intact organisms

 

captured from the wild; no isogenic lines; there is a facility that breeds and rears Aplysia at U. Miami

     
     

Special Strengths

gene transfer simple and efficient; great background knowledge of embryo molecular and cell biology; large assemblage of clones libraries, probes available; genomics; advanced technology for molecular biology of gene regulation; ease of culture of embryo and adults; enormous fecundity; rapid, simple embyogenesis; long-lived; hardy adult form.

relatively simple nervous system; only 20,000 neurons; big neurons/few cells; well defined circuitry that can be reconstituted in culture; demonstrates multiple forms of synaptic plasticity; relating individual cells to behavior easy; functional characterization of genes, relating genes to specific neuronal function and neuronal placticity in individual indentified cells that are causally related to behavior and learning possible; genes important for memory and for motivational state

     

Weaknesses

long egg to egg life cycle; no cell culture

no isogenic strains; no classical whole animal genetics

     

Resources

SUMS at Cal Tech; arrayed libraries

U. of Miami Marine Facility

     

Databases

Stowers Genome Project (in preparation); EST database

Database of Identified Cell Anatomy, Physiology, and Behavior (Dan Gardner; http://mollusc.med.cornell.edu; ~20%-40% of whole CNS is identified and characterized functionally

     

Community

   

# of labs

>50 (US, Japan, France, Italy, Russia)

70-80 all working on nervous system and behavior

# of investigators

>500

200-300

     
     

References

E. H. Davidson, R. A. Cameron, A. Ransick (1998). Specification of cell fate in the sea urchin embryo: summary and some proposed mechanisms. Development 125, 3269-3290.

C.-H. Yuh, H. Bolouri, E. H. Davidson (1998). Genomic cis-regulatory logic: functional analysis and computational model of a sea urchin gene control system. Science 279, 1896-1902. ed.

DeZazzo, J. & Tully, T (1995). Dissection of memory formation. From behavioral pharmacoloty to molecular genetics. Trends Neurosci. 18:212-218.

Bailey, C.H., Bartsch, D. & Kandel, E.R. (1996). Toward a molecular definition of long-term memory storage. PNAS USA 93: 13445-13425.

Kandel, E.R. (1979). The Behavioral Biology of Aplysia: A Contribution to the comparative Study of Opisthobranch Molluscs. San Francisco: Freeman

Information Provided By:

E. Davidson

E. Kandel

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