Skip Navigation Genome.gov - National Human Genome Research InstituteGenome.gov - National Human Genome Research InstituteGenome.gov - National Human Genome Research InstituteNational Institutes of Health
   
       Home | About NHGRI | Newsroom | Staff
Research Grants Health Policy & Ethics Educational Resources Careers & Training

Home>Educational Resources>Online Education Kit: Understanding the Human Genome Project>Online Education Kit: Timeline >Online Education Kit: 1981-82: First Transgenic Mice and Fruit Flies
Print Version


 Timeline:
 1800s                  
 1900s                  
 1940s                  
 1950s                  
 1960s                  
 1970s                  
 1980s                  
 1990 - 1994        
 1995 - 1996        
 1997 - 1999        
 2000 - 2001        
 2002 - 2003        
 2004 - Future    


Return to Online
Education Kit

Previous Event Previous Event | Next Event Next Event

1981-82: First Transgenic Mice and Fruit Flies

Photo of a laboratory mouse Scientists had been able to add new genes to bacterial cells for several years. In the early 1980s, they figured out how to add stably-inherited new genes to animals. The first such "transgenic animals" were mice and fruit flies. By adding foreign genes or genes spelled slightly differently than normal, scientists had a new way to test the functions of genes.

More Information

References for Adding Genes to Mice:

Costantini F., Lacy E. Introduction of a rabbit beta-globin gene into the mouse germ line. Nature, 294(5836):92-4. 1981. [PubMed]

N&V: Hogan, B., Williams, J. Integration of foreign genes into the mammalian germ line: genetic engineering enters a new era. Nature, 294(5836):9-10. 1981. [PubMed]

Gordon, J.W., Ruddle, F.H. Integration and stable germ line transmission of genes injected into mouse pronuclei. Science, 214(4526):1244-6. 1981. [PubMed]

Abstract: Genetic material has been successfully transferred into the genomes of newborn mice by injection of that material into pronuclei of fertilized eggs. Initial results indicated two patterns of processing the injected DNA: one in which the material was not integrated into the host genome, and another in which the injected genes became associated with high molecular weight DNA. These patterns are maintained through further development to adulthood. The evidence presented indicates the covalent association of injected DNA with host sequences, and transmission of such linked sequences in a Mendelian distribution to two succeeding generations of progeny.

Reference for Adding Genes to Flies:

Rubin, G.M., Spradling A.C. Genetic transformation of Drosophila with transposable element vectors. Science, 218(4570):348-53. 1982. [PubMed]

Adding Genes to FlyAbstract: Exogenous DNA sequences were introduced into the Drosophila germ line. A rosy transposon (ry1), constructed by inserting a chromosomal DNA fragment containing the wild-type rosy gene into a P transposable element, transformed germ line cells in 20 to 50 percent of the injected rosy mutant embryos. Transformants contained one or two copies of chromosomally integrated, intact ry1 that were stably inherited in subsequent generations. These transformed flies had wild-type eye color indicating that the visible genetic defect in the host strain could be fully and permanently corrected by the transferred gene. To demonstrate the generality of this approach, a DNA segment that does not confer a recognizable phenotype on recipients was also transferred into germ line chromosomes.

 

 

 

 

 

 

Previous Event Previous Event | Next Event Next Event

Top of page

Last Reviewed: April 15, 2008


PrivacyCopyrightContactAccessibilitySite MapStaff DirectoryFOIAHome Department of Health and Human Services  National Institutes of Health  USA.gov