Emphasis should be laid on the possible drug etiology in any patient who develops new signs and symptoms while on medications, even if it may not be supported by enough literature.”
“Spinocerebellar ataxia type 1 (SCAl) is a dominant inherited disease caused by expanded trincleotide repeats resulting in an increased polyglutamine tract in the gene product. As a potential therapeutic approach for SCAl we tested antisense RNAs targeting two regions of the ataxin-l message. Single-stranded

regions around the translational initiation site and the intron 8 splice donor site of the ataxin-1 message were YH25448 manufacturer identified by computer-assisted RNA secondary structure prediction. Plasmids were generated to contain a 254-bp antisense

sequence spanning the translation initiation site (pLasBDini) or a 317-bp sequence spanning the intron 8 splice donor site (pLasBDei) of the ataxin-l message. These plasmids were transfected into Chinese bamster ovary cells engineered to express either expanded Or unexpanded ataxin-1 message and protein. Reduced levels of mutant ataxin-1 message (82 CAG repeats), wild-type ataxin-1 message (30 CAG repeats), and ataxin-1 protein were observed by Northern and Western Not analyses in pLasBDini-transfected clones. pLasBDei-transfected 293 cells exhibited a shift in ataxin-1 message to a size several kilobases longer than that of the natural message. Reverse transcriptase/polymerase chain reaction Selleck CDK inhibitor assays demonstrated the retention of message spanning the intron 8 splice SBC-115076 chemical structure acceptor and the inability to amplify sequences between exons 8 and 9, implying that normal splicing of intron 8 had been interrupted. We conclude that antisense RNAs were effective in reducing or modifying ataxin-1 messages in transfected cells, and may be an effective genetic strategy for therapy of SCAl and similar dominant-acting neurological disorders.”
“Cryptosporidium parvum is a member of the Apicomplexa that lacks a plastid and associated

nuclear-encoded genes, which has hampered its use in evolutionary comparisons with algae and eliminated a pool of potentially useful drug targets. Here we show that apicomplexan parasites possess an unusual family of class II histone deacetylase (HDAC) proteins with orthologues that are present in other chromalveolates and primitive algae. A striking feature of these HDAC proteins is the presence of ankyrin repeats in the amino-terminus that appear to be required for enzyme activity. In vitro and in vivo analyses of the C. parvum orthologue indicate that this subclass of chromatin-remodel ling proteins is targeted by the anti-cancer drug suberoylanilide hydroxamic acid and that these proteins are most likely involved in the essential process of H4 histone deacetylation that coincides with DNA replication.