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1.
Neuroimage ; 56(4): 2209-17, 2011 Jun 15.
Article in English | MEDLINE | ID: mdl-21421063

ABSTRACT

Patients with childhood absence epilepsy (CAE) often demonstrate impaired interictal attention, even with control of their seizures. No previous study has investigated the brain networks involved in this impairment. We used the continuous performance task (CPT) of attentional vigilance and the repetitive tapping task (RTT), a control motor task, to examine interictal attention in 26 children with CAE and 22 matched healthy controls. Each subject underwent simultaneous 3T functional magnetic resonance imaging-electroencephalography (fMRI-EEG) and CPT/RTT testing. Areas of activation on fMRI during the CPT task were correlated with behavioral performance and used as seed regions for resting functional connectivity analysis. All behavioral measures reflecting inattention were significantly higher in patients. Correlation analysis revealed that impairment on all measures of inattention on the CPT task was associated with decreased medial frontal cortex (MFC) activation during CPT. In addition, analysis of resting functional connectivity revealed an overall decrease within an 'attention network' in patients relative to controls. Patients demonstrated significantly impaired connectivity between the right anterior insula/frontal operculum (In/FO) and MFC relative to controls. Our results suggest that there is impaired function in an attention network comprising anterior In/FO and MFC in patients with CAE. These findings provide an anatomical and functional basis for impaired interictal attention in CAE, which may allow the development of improved treatments targeted at these networks.


Subject(s)
Attention/physiology , Brain Mapping/methods , Brain/physiopathology , Epilepsy, Absence/physiopathology , Neural Pathways/physiopathology , Adolescent , Child , Electroencephalography , Female , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Psychomotor Performance/physiology , Signal Processing, Computer-Assisted , Young Adult
2.
Genes Dev ; 20(24): 3407-25, 2006 Dec 15.
Article in English | MEDLINE | ID: mdl-17182867

ABSTRACT

To better understand the diversity of small silencing RNAs expressed in plants, we employed high-throughput pyrosequencing to obtain 887,000 reads corresponding to Arabidopsis thaliana small RNAs. They represented 340,000 unique sequences, a substantially greater diversity than previously obtained in any species. Most of the small RNAs had the properties of heterochromatic small interfering RNAs (siRNAs) associated with DNA silencing in that they were preferentially 24 nucleotides long and mapped to intergenic regions. Their density was greatest in the proximal and distal pericentromeric regions, with only a slightly preferential propensity to match repetitive elements. Also present were 38 newly identified microRNAs (miRNAs) and dozens of other plausible candidates. One miRNA mapped within an intron of DICER-LIKE 1 (DCL1), suggesting a second homeostatic autoregulatory mechanism for DCL1 expression; another defined the phase for siRNAs deriving from a newly identified trans-acting siRNA gene (TAS4); and two depended on DCL4 rather than DCL1 for their accumulation, indicating a second pathway for miRNA biogenesis in plants. More generally, our results revealed the existence of a layer of miRNA-based control beyond that found previously that is evolutionarily much more fluid, employing many newly emergent and diverse miRNAs, each expressed in specialized tissues or at low levels under standard growth conditions.


Subject(s)
Arabidopsis/genetics , MicroRNAs/genetics , Arabidopsis Proteins/metabolism , Base Sequence , Cell Cycle Proteins/metabolism , DNA, Complementary , Gene Expression Regulation, Plant , Gene Library , MicroRNAs/chemistry , Molecular Sequence Data , Nucleic Acid Conformation , RNA, Plant/chemistry , RNA, Plant/genetics , RNA, Small Interfering/chemistry , RNA, Small Interfering/genetics , Ribonuclease III/metabolism , Ribonucleases/metabolism , Sequence Analysis, RNA
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