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Fruit fly (Drosophila melanogaster

D. melanogsater genome facts:
sequenced 2001
1.3 million base pairs
13,000 genes




↓ general and genome resource links ↓

 
Drosophila melanogaster
Drosophila melanogaster

About the Fruit fly:

With a history of study of almost a century, the fruit fly Drosophila melanogaster is perhaps the best characterized multicellular organism. The fly was first studied by Thomas Hunt Morgan, an American embryologist at Columbia University, in order to try to understand the mechanisms of inheritance and the role of genes in this process. As such, it was the first genetic model organism, and over its long history of use in the lab, a dazzling array of genetic tools and techniques have been developed to facilitate laboratory study.

D. melanogaster close up
D. melanogaster close up
As a genetic model organism, fruit flies have several attractive characteristics: they are small, easy to keep in a laboratory setting, and have a short generation time. Flies have served as an important tool in the study of an abundance of biological process, including development, the cell cycle, and behavior. Studies of flies led to such fundamental concepts as the role of chromosomes in inheritance

The genome of D. melanogaster has been sequenced and available since 1999. Preliminary analysis of the genome showed a close correspondence to the genomes of vertebrates such as mouse and human; about 60 percent of genes are conserved between fly and human. However, compared to vertebrates, the fly has a relatively compact genome, meaning that there is relatively less noncoding sequence. The reduced complexity of the noncoding regions allows for easier determination of their roles in the regulation of gene expression.

Studies at CIG are currently focused on the noncoding regions of D. melanogaster, as well as a number of Drosophila subspecies. Comparing the genomes of these closely related species will allow for the identification of conserved regulatory sequences, and examination of networks of these regulatory regions will facilitate our understanding of how complex genetic programs of multicellular organisms are enacted.

 


CIG faculty who study me:

Sandrine Dudoit

Michael Eisen

Donald Rio

Robert Tjian

Michael Levine


Related research projects: