BaNG - Blaxter Nematode and Neglected Genomics
  The C. elegans genome
     Introduction to the genome of a model nematode
       Mark Blaxter at the Institute of Evolutionary Biology, University of Edinburgh
How was the genome sequenced?
Annotating the genome
 

Expressed sequence tags (ESTs) from Caenorhabditis elegans

An expressed sequence tag is a single pass sequence taken from a randomly selected cDNA clone. ESTs are used to investigate the diversity of genes expressed by an organism, tissue or cell. By looking at only expressed sequences we can

  • avoid the expense of complete genome sequencing (no introns or intergenic DNA are sequenced)
  • allow the organism/tissue/cell to instruct us as to what is "important" in terms of expression levels of genes
  • permit assessment of differential gene expression by comparing stage or tissue specific datasets
  • confirm splicing and coding predictions from genomic DNA sequences

For C. elegans there are three sources of ESTs. Two small (~1300 sequence) datasets were produced early in the genome project, one by TIGR and the other by Washington University. However, the vast majority of ESTs have been produced by the lab of Yuji Kohara in Japan. To date (2007) over 300,000 ESTs have been deposited by Prof. Kohara's lab in public databases.

The "Orfeome Project" has also attempted to define the transcriptome of C. elegans by PCR amplifying from cDNA using primenrs predicted to span genes in the genome sequence (called "ORF" or open reading frame sequences).

A third sequence-based method that has been used to define and analyse the C. elegans transcriptome is serial analysis of gene expression (SAGE). Expression levels of predicted genes have also been defined using microarrays.

 

 

 

 

 

 

 

 

 

 

 

These pages were written by Mark Blaxter and last updated in early 2007.
Contact the www.nematodes.org webmaster if there are problems.