Genetics: CA10

I've been wondering- if CA10 is involved in ME/CFS (or pain disorders) could it (or whatever mechnistic process the CA10 gene finding represents) be directly modulated with drugs in order to stop whatever signals are causing PEM/pain etc? Or is it more of a pointer to the general pathology
 
Inspired by some AlphaGenome stuff I’ve been learning more about and am interested in looking at promoters and enhancers for some of these candidate genes.

Enhancers and promoters are gene-regulatory elements. They are stretches of DNA that help in both eukaryotic and prokaryotic transcription. The promoters are known to initiate transcription, and the enhancers increase the level of transcription
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If you look at the genecard for CA10 in the genomics section you can see GeneHancer info on these. There’s lots of interesting stuff in there.

For instance pick the top one, a promoter/enhancer with a high score (it has a little star by it to show this too)
Expand the info and see the location of it is chr17:52158438-52159092
You can zoom in to that location on the DecodeME LocusZoom data and see lots of the hits tie in with this area
The Ensembl info has which tissues these are active in too
Looking at details of all of them a number match with the changes on DecodeME

If I’m interpreting this right it says the changes people with ME/CFS are more likely to have are in these promoters and enhancers in those tissues? So affect expression of CA10 in those tissues? Is that right?

Sorry if this is covering known territory, it’s all new to me. Given the location, at the start of the transcription site, it may be obvious to people thst these are promoters?

I wonder if it’s worth digging through all the Genhancer info for all the genes, especially as some enhancers can be a long way away from the transcription site for the gene.

The EPDnew info will look familiar to anyone who has been looking at AlphaGenome outputs too… I have lots more to learn here.
 
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@hotblack you might like to explore some of the tracks on UCSC genome browser--it compiles a lot of this information visually so you can do some exploring.

Here I have it centered on the top DecodeME SNP in the region:

You can "highlight" a region by dragging a box over a region and clicking "add highlight" on the box that comes up, that way you can keep track of where a SNP overlaps with features on other tracks
1770839351753.png

These tracks have a lot of promoter/enhancer/regulatory region info you can play around with (click "show" and then "refresh" to add them.
1770839478359.png

The GENCODE track under "Genes and Gene Predictions" will mark known genes with their exons and introns

If you want to highlight a lot of SNPs at once there are ways you can add a custom track in a BED file format, though it'll take more effort to figure out
 
@hotblack you might like to explore some of the tracks on UCSC genome browser--it compiles a lot of this information visually so you can do some exploring.
Thanks! The highlighting doesn’t seem very touchscreen friendly unfortunately. But the rest seems to work, I’ll have an explore.
 
Thanks! The highlighting doesn’t seem very touchscreen friendly unfortunately. But the rest seems to work, I’ll have an explore.
If you start zoomed in on a SNP, you can also hit the "highlight" button down here which will highlight everything in your viewer

1770841533760.png
 
For instance pick the top one, a promoter/enhancer with a high score (it has a little star by it to show this too)
Expand the info and see the location of it is chr17:52158438-52159092
You can zoom in to that location on the DecodeME LocusZoom data and see lots of the hits tie in with this area

This is more or less exactly what my genetics friends at UCL did when they gave me a presentation of why they thought it was worth picking CA10 for a basic biology project.
 
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