- Golden Corral coming to Cape; may hire 100 workers (7/21/16)9
- Arrest warrants filed for six drug suspects in Cape (7/19/16)6
- Area groups working together to reintroduce elk in Missouri (7/18/16)1
- Suspect in downtown Cape shooting ID'd in court (7/20/16)2
- Prosecutor says shooting by state trooper was justified (7/24/16)15
- Hastings in Cape closing (7/22/16)5
- Governor signs Rep. Swan bill that equalizes child-custody criteria (7/6/16)5
- City may spend extra park tax money on Cape Splash, skate park, other projects (7/25/16)10
- Jackson's former police dog euthanized Monday (7/21/16)2
- 'I want to see how far I can go' (7/21/16)2
Scientists complete comprehensive physical map of mouse genome
LOS ANGELES -- An international team has completed the most comprehensive map ever of the genetic code of the mouse, an accomplishment that will make the laboratory animal more useful to scientists studying human health and disease.
The map covers an estimated 98 percent of the order of the nearly 3 billion letters that make up the mouse code, or genome.
Two efforts have nearly completed the deciphering of those letters, and the map will serve as an atlas of the genome and allow scientists to zero in on regions of interest. It will also permit scientists to fill in gaps that remain in the deciphering efforts, which remain in draft form.
Details are to appear Monday in the online edition of the journal Nature. The map is available for public review on the Internet.
Humans and mice last shared a common ancestor -- probably a small rodentlike mammal -- roughly 100 million years ago, but today retain similar-sized genomes and many of the same genes. That makes mice ideal stand-ins for humans in genetic studies.
The function of many human genes, much less the role they play in disease, is unknown.
Creating so-called "knockout mice" -- animals whose genetic code has been altered in the lab to either turn on or off certain genes that mice and humans share -- allows scientists to understand the purpose of those genes and their role in disease, as well as test therapeutic drugs.
"Now that we have the human sequence, it's trying to interpret what's actually contained in it. A lot of genes in the human we don't have a function for them. If we are able to map them in a model organism like the mouse, we can derive their function by knocking them out," said study co-author Simon Gregory of the Wellcome Trust Sanger Institute in Cambridge, England. The team also included scientists from various research institutes and universities in Canada and the United States.