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A risk variant reportedly creates a new CTCF site

A post says Oxford’s MCCv maps chromatin at base-pair and single-allele resolution, with findings from 405 immune enhancers.

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1 Source, 17h ago, first seen 17h ago

TLDR

A post says Oxford’s MCCv maps chromatin at base-pair and single-allele resolution. It says researchers found a risk variant among 405 immune enhancers that creates a new CTCF site and blocks SESN3, linking the change to autoimmunity via tryptophan and mTOR.

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79

1 Source, first seen 17h ago

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Combined views

79

1 Source, first seen 17h ago

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1 Source

@GinasassyassScience News: Scientists can now watch one disease DNA letter rewrite genome wiring. Oxford’s MCCv maps chromatin at base pair, single allele resolution. In 405 immune enhancers they found a risk variant that creates a neo CTCF site, blocks SESN3, and fuels autoimmunity via tryptophan mTOR. Eventually we'll live forever, maybe.17h
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    1 Source

    @GinasassyassScience News: Scientists can now watch one disease DNA letter rewrite genome wiring. Oxford’s MCCv maps chromatin at base pair, single allele resolution. In 405 immune enhancers they found a risk variant that creates a neo CTCF site, blocks SESN3, and fuels autoimmunity via tryptophan mTOR. Eventually we'll live forever, maybe.17h
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