Author Archives: Smithy

Functional annotation of your long non-coding RNA

So you have performed some differential gene expression experiments and have discovered a (few) non-coding RNAs that are of conspicuous interest… What now? Unless you are lucky and someone else has already characterised your needle in a haystack, odds are little is known about this transcript. You might be tempted to paste that .fasta file into mfold and say: “Look! It folds into an RNA secondary structure!” yet this won’t tell you much, besides that your RNA might look like a Christmas tree in February. This video explains how you can find out which regions of your RNA transcript of interest might be responsible for its biological function.

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by | August 27, 2013 · 6:37 am

A novel role for Alu elements in epigenetic trans-regulation of gene networks

Screen Shot 2013-07-26 at 9.42.44 PMEver so often, you stumble across a magnificent work of science. This was the case for me a few weeks ago when this work popped up in my news feed. The authors investigate how a genomic locus that is the strongest risk factor for artherosclerosis produces a regulatory non-coding gene that regulates other genes associated to the disease.

They used stable over-expression and knock-down approaches to investigate the role of distinct ANRIL (a long non-coding RNA, aka lncRNA) isoforms in several key mechanisms of atherogenesis. They show that this gene guides epigenetic effector complexes to specific genomic loci.

Through what molecular mechanism you ask? None other than via endogenous transposable elements–ALUs specifically–that have been harnessed through evolution to perform regulation of gene expression in our genomes. FYI, repetitive elements compose ~46% of the human genome, 20% of which are ALUs.
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Evolutionary proof that much of our genome is functional

RNA2DEVOLast year, the massive ENCODE consortium disclosed that over 80% of the human genome appears to be functional through several detailed biochemical experiments. Their findings fuelled an already heated debate regarding the biological pertinence of similar findings. Many old-school biochemists and proponents of the “selfish” DNA hypothesis (who I collectively refer to as junk DNAy-sayers) dismiss the use of such data to support the notion that the majority of the genome is functional.

Amidst the nit-picking, bickering, and refutations, one logical argument stands out that somewhat confounds the ENCODE findings: the lack of detectable evolutionary conservation. Indeed, the statement that > 80% of the human genome sequence is biologically functional lies in stark contrast to the fact that < 9% of it is observed to be conserved throughout mammalian evolution. But is this estimate really accurate? Continue reading

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Some praise for Dr Mercer’s work on the blogosphere (Dr. Mary Mangan @ Open Helix Blog). Video Tip of the Week: Mitochondrial transcriptome GBrowser

Perhaps something like Chromozoom might make it easier to visualize transcriptomic data for smaller genomes. Did I just criticize our own work? SNAP!

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by | May 13, 2012 · 2:41 pm

First post

The basics are up and running.

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by | May 9, 2012 · 2:46 pm