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TIGR, Sanger Say Diarrhea Amoeba Nastier Than Thought

NEW YORK, Feb. 23 (GenomeWeb News) - The Institute for Genomic Research and the Wellcome Trust Sanger Institute have learned that a parasitic amoeba that causes severe diarrheal disease in developing countries has a combination of sensory genes and bacteria-like genes that make its biology unusual.

 

The two institutes will publish the results of their findings on the genome sequence of Entamoeba histolytica in the Feb. 24 issue of Nature in what they claim is the first genome-wide study of an amoeba and the first genome sequence to be published from this amoeba's class of amitochondrial human pathogens.

 

The duo of institutes expect the genome sequence to help in the development of new vaccines as well as diagnostic tests that can distinguish the amoeba's most deadly strains. The two say E. histolytica, which causes a disease called amebiasis, infects an estimated 50 million people and causes as many as 100,000 deaths a year -- second only to malaria as a cause of morbidity and mortality from a protist.

 

The research that led to the discovery was funded by grants from Wellcome Trust and the National Institutes of Health.

The Scan

LINE-1 Linked to Premature Aging Conditions

Researchers report in Science Translational Medicine that the accumulation of LINE-1 RNA contributes to premature aging conditions and that symptoms can be improved by targeting them.

Team Presents Cattle Genotype-Tissue Expression Atlas

Using RNA sequences representing thousands of cattle samples, researchers looked at relationships between cattle genotype and tissue expression in Nature Genetics.

Researchers Map Recombination in Khoe-San Population

With whole-genome sequences for dozens of individuals from the Nama population, researchers saw in Genome Biology fine-scale recombination patterns that clustered outside of other populations.

Myotonic Dystrophy Repeat Detected in Family Genome Sequencing Analysis

While sequencing individuals from a multi-generation family, researchers identified a myotonic dystrophy type 2-related short tandem repeat in the European Journal of Human Genetics.