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Genome Biology 2005, 6(3):314
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Recommended
F1000 Factor 3.0


Architecture of a validated microRNA::target interaction.
Vella MC, Reinert K, Slack FJ
Chem Biol 2004 Dec 11(12):1619-23 [
abstract on PubMed][request from library]
Selected by | Isaac Kohane
Evaluated 15 Feb 2005

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Faculty Member Comments
Isaac Kohane
Harvard Medical School, Children's Hospital, United States of America
PHYSIOLOGY


New Finding
In the context of all the bioinformatics search algorithms for miRNA targets/binding sites, this paper helps cast the light of empiricism on some of these results. An in vivo assay is used to explore the downregulation of a target gene of a nematode miRNA. It appears that there is considerably more complexity in the effective downregulation of the target beyond the immediate region of complementarity (i.e. the context of the target site does matter); however, it is unclear to what extent the findings here can be generalized.

Evaluated 15 Feb 2005

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Evidence for Widespread Degradation of Gene Control Regions in Hominid Genomes.
Keightley PD, Lercher MJ, Eyre-Walker A
PLoS Biol 2005 Jan 25 3(2):e42 [
abstract on PubMed] [FREE full text]
Selected by | Molly Przeworski
Evaluated 9 Feb 2005

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Faculty Member Comments
Molly Przeworski
Brown University, United States of America
GENOMICS & GENETICS


Controversial
This large-scale analysis of ape and rodent genomes yields little or no evidence for natural selection (either positive or purifying) acting on non-protein-coding regions of the human genome. In contrast, there is evidence for purifying selection on these regions in murid genomes. This finding suggests that the smaller effective population size of humans may render selection ineffective at purging mildly deleterious alleles.

Evaluated 9 Feb 2005

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Small molecule control of pre-mRNA splicing.
Graveley BR
RNA 2005 Jan 20 [
abstract on PubMed] [request from library]
Selected by | Lawrence Chasin
Evaluated 16 Feb 2005

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Faculty Member Comments
Lawrence Chasin
University of Texas, United States of America
CELL BIOLOGY


Tech Advance
This paper describes the engineering of a splicing substrate and 2 splicing factor fusion proteins such that splicing is dependent on the presence of a rapamycin derivative bringing the 2 splicing factors domains together. This ability to turn on splicing with a small molecule may be useful for studying the kinetics of splice site recognition. If it can be extended to cells, it should prove useful in evaluating the roles of protein splicing isoforms.

Evaluated 16 Feb 2005

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Trypanosoma brucei RNA interference in the mammalian host.
Lecordier L, Walgraffe D, Devaux S, Poelvoorde P, Pays E, Vanhamme L
Mol Biochem Parasitol 2005 Mar 142(1):127-31 [
abstract on PubMed] [request from library]
Selected by | Michael Cappello
Evaluated 14 Feb 2005

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Faculty Member Comments
Michael Cappello
Yale University School of Medicine, United States of America
MICROBIOLOGY


New Finding
Tech Advance
This paper demonstrates the potential to induce gene silencing of Trypanosoma brucei via RNA interference within a mammalian host. Mice infected with trypanosomes transfected with an inducible plasmid vector allowing for production of gene-specific dsRNA demonstrated a transient suppression of parasitemia and prolonged survival compared to controls. Although the effect was transient, these data support the concept that RNAi can be utilized in vivo to characterize the role of specific gene products in pathogenesis.

Evaluated 14 Feb 2005

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Simultaneous genotyping, gene-expression measurement, and detection of allele-specific expression with oligonucleotide arrays.
Ronald J, Akey JM, Whittle J, Smith EN, Yvert G, Kruglyak L
Genome Res 2005 Feb 15(2):284-91 [
abstract on PubMed] [request from library]
Selected by | Karin Schmitt
Evaluated 10 Feb 2005

Faculty Comments
Faculty Member Comments
Karin Schmitt
Open Biosystems, United States of America
GENOMICS & GENETICS


Tech Advance
This is the first paper describing the use microarrays to simultaneously measure gene expression, genotype and detect allele-specific expression, based on the hybridization of mRNA to a microarray. Studies in yeast are presented in a proof-of-principle experiment. The method has some disadvantage (for example: relying on reduced marker density for genotyping) and a high false positive rate for allele-specific expression but overall presents an interesting approach.

Evaluated 10 Feb 2005













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