Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a228a19fed898821

Jump to content

// Workers AI · dad joke modeWhat did HT-TALENS say to its friend? "You're a real thread

From Wikipedia, the free encyclopedia

HT-TALENS (HIV-targeted transcription activator-like effector nucleases) is an engineered plant protein that is a proposed cure for AIDS.[1][2]

AIDS

[edit]

The HIV genome is made from RNA rather than DNA. The enzyme that converts RNA to DNA and then inserts it into a cell makes between one and 10 mistakes every time it copies itself. This high error rate means that the virus population that inhabits each HIV patients is genetically diverse.[1]

When the HIV virus infects someone, it copies its DNA and inserts into the DNA of white blood cells, making the virus part of its host. Even if these genes could be silenced with drugs, (later) stopping the drugs sets the viral DNA free to attack the patient.[1]

HT-TALENs binds to that sequence and cuts the HIV DNA, but not human DNA. When that cut gets fixed by the cell's DNA repair system, it makes a scar that leaves the virus unable to return and make HIV DNA cells. 60% of the cells making the protein damage the viral DNA.[1]

See also

[edit]

References

[edit]
  1. 1 2 3 4 Hock, Lindsay (October 5, 2015). "Gene-editing Technique Stops AIDS Virus in its Tracks". Research & Development. Retrieved 2015-10-09.
  2. Strong, Christy L.; Guerra, Horacio P.; Mathew, Kiran R.; Roy, Nervik; Simpson, Lacy R.; Schiller, Martin R. (2015-05-06). "Damaging the Integrated HIV Proviral DNA with TALENs". PLOS ONE. 10 (5) e0125652. Bibcode:2015PLoSO..1025652S. doi:10.1371/journal.pone.0125652. PMC 4422436. PMID 25946221.