Artistic representation of events occurring during gene silencing in Fragile X mental retardation syndrome (FXS). The FMR1 gene, which is on the X chromosome, colocalizes with a fragile site seen in FXS cells that gives this disorder its name. FXS alleles become associated with SIRT1. SIRT1, a class III histone deacetylase, deacetylates lysine 9 of histone H3 and lysine 16 of histone H4, ultimately leading to chromatin compaction and gene silencing (see Biacsi et al., e1000017).
Image Credit: Image by Dr. Marian L. Miller (Journal-Cover-Art.com).
Interview
Imagine: An Interview with Svante Pääbo
PLOS Genetics: published March 28, 2008 | https://doi.org/10.1371/journal.pgen.1000035
Research Articles
ruvA Mutants That Resolve Holliday Junctions but Do Not Reverse Replication Forks
PLOS Genetics: published March 7, 2008 | https://doi.org/10.1371/journal.pgen.1000012
GADD45A Does Not Promote DNA Demethylation
PLOS Genetics: published March 7, 2008 | https://doi.org/10.1371/journal.pgen.1000013
Role of Duplicate Genes in Robustness against Deleterious Human Mutations
PLOS Genetics: published March 14, 2008 | https://doi.org/10.1371/journal.pgen.1000014
Transcription and Chromatin Organization of a Housekeeping Gene Cluster Containing an Integrated β-Globin Locus Control Region
PLOS Genetics: published March 7, 2008 | https://doi.org/10.1371/journal.pgen.1000016
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PLOS Genetics: published March 14, 2008 | https://doi.org/10.1371/journal.pgen.1000017
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PLOS Genetics: published March 7, 2008 | https://doi.org/10.1371/journal.pgen.1000018
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An Abundant Evolutionarily Conserved CSB-PiggyBac Fusion Protein Expressed in Cockayne Syndrome
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