slik Gene Controls Cell Growth and Survival

Affordable Access

slik Gene Controls Cell Growth and Survival

Publisher
Public Library of Science
Publication Date
Nov 01, 2003
Source
PMC
Keywords
Disciplines
  • Biology
  • Medicine
License
Unknown

Abstract

PLBI0102_fmi-165.indd Volume 1 | Issue 2 | Page 135PLoS Biology | http://biology.plosjournals.org Research Digest Synopses of Research Articles Caenorhabditis elegans, a 1-mm soil-dwelling roundworm with 959 cells, may be the best-understood multicellular organism on the planet. As the most “pared-down’’ animal that shares essential features of human biology—from embryogenesis to aging—C. elegans is a favorite subject for studying how genes control these processes. The way these genes work in worms helps scientists understand how diseases like cancer and Alzheimer’s develop in humans when genes malfunction. With the publication of a draft genome sequence of C. elegans’ first cousin, C. briggsae, Lincoln Stein and colleagues have greatly enhanced biologists’ ability to mine C. elegans for biological gold. Every organism carries clues to its molecular operating system and evolutionary past embedded in the content and structure of its genome. To unearth these clues, scientists examine different regions of the genome, assembling data on sequences, genes, functional elements that are not genes (but that regulate them, for example), repeated sequences, and so on. By comparing the genomes of related organisms, researchers can see what parts of the genomes are conserved—highly conserved genes tend to be important—and then focus on these regions to track down genes and determine how they function. To construct a draft sequence of the C. briggsae genome, the researchers merged genomic data from three sources—one derived from whole-genome shotgun sequencing, another from physical genome mapping, and the third from regions of a previously “finished’’ sequence. For the shotgun sequence, the researchers extracted DNA from worms, randomly cut it into short pieces, sequenced them, and then assembled overlapping sequences to create thousands of stretches of contiguous DNA sequence. To help fill in the gaps between these “contigs,’’ Stein and colleagues deve

Report this publication

Statistics

Seen <100 times