<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Genome-Engineering on Bioecon</title><link>https://en.bioecon.ru/clusters/genome-engineering/</link><description>Recent content in Genome-Engineering on Bioecon</description><generator>Hugo</generator><language>en-US</language><lastBuildDate>Fri, 24 Jul 2026 01:47:15 +0700</lastBuildDate><atom:link href="https://en.bioecon.ru/clusters/genome-engineering/index.xml" rel="self" type="application/rss+xml"/><item><title>Biosafety &amp; lab biosecurity</title><link>https://en.bioecon.ru/technology/biosafety-lab-biosecurity/</link><pubDate>Thu, 23 Jul 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/biosafety-lab-biosecurity/</guid><description>Physical-containment infrastructure — biological safety cabinets, HEPA filtration, autoclave sterilization and BSL-1 to BSL-4 containment — that protects personnel, product and environment in every biotechnology laboratory, governed by NSF/ANSI 49 and EN 12469.</description></item><item><title>Ecological engineering &amp; gene drives</title><link>https://en.bioecon.ru/technology/ecological-engineering-gene-drives/</link><pubDate>Mon, 06 Jul 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/ecological-engineering-gene-drives/</guid><description>Deliberately engineering whole wild populations — from CRISPR gene drives that force 100% inheritance of a trait through a mosquito population in 6-20 generations to Wolbachia-infected and radiation-sterilized releases that collapse it instead — as a genetic complement to nature-based ecological engineering like constructed wetlands and living shorelines, all governed by an irreversibility problem no field release can undo.</description></item><item><title>Intelligent genetic switches (kill switches)</title><link>https://en.bioecon.ru/technology/intelligent-genetic-switches-kill-switches/</link><pubDate>Sun, 05 Jul 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/intelligent-genetic-switches-kill-switches/</guid><description>Synthetic gene circuits that force engineered organisms to depend on external chemical signals for survival, self-destructing or losing viability once released into the environment — the biocontainment standard now required before any regulator clears a synthetic-biology product for open-system field trials.</description></item><item><title>Xenobiology &amp; expanded genetic alphabet (XNA)</title><link>https://en.bioecon.ru/technology/xenobiology-expanded-genetic-alphabet/</link><pubDate>Sun, 05 Jul 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/xenobiology-expanded-genetic-alphabet/</guid><description>Orthogonal biological systems built on xeno-nucleic acids, unnatural base pairs and genomically recoded organisms that incorporate noncanonical amino acids into proteins — enabling site-specific drug conjugation and a genetic firewall against horizontal gene transfer with wild species.</description></item><item><title>Epigenome editing</title><link>https://en.bioecon.ru/technology/epigenome-editing/</link><pubDate>Fri, 03 Jul 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/epigenome-editing/</guid><description>Turning genes on or off by rewriting DNA methylation and histone marks with dCas9 fusion proteins or zinc fingers — no DNA sequence change, but an effect that can be inherited across cell divisions.</description></item><item><title>Minimal genomes &amp; synthetic cells</title><link>https://en.bioecon.ru/technology/minimal-genomes-synthetic-cells/</link><pubDate>Fri, 26 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/minimal-genomes-synthetic-cells/</guid><description>The frontier of building life de novo — stripping genomes down to a minimal viable chassis (top-down) and assembling artificial cells from non-living parts (bottom-up) to make predictable, biocontained cell factories.</description></item><item><title>Prime editing</title><link>https://en.bioecon.ru/technology/prime-editing/</link><pubDate>Fri, 26 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/prime-editing/</guid><description>Search-and-replace genome editing with a Cas9 nickase fused to a reverse transcriptase and an extended pegRNA — writing all 12 base substitutions and small indels without a double-strand break.</description></item><item><title>Synthetic biology</title><link>https://en.bioecon.ru/technology/synthetic-biology/</link><pubDate>Fri, 26 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/synthetic-biology/</guid><description>The engineering of biology — designing DNA, cells and genetic circuits on computers, building them in biofoundries and scaling them into chemicals, materials and ingredients through the Design-Build-Test-Learn cycle.</description></item><item><title>Genome editing</title><link>https://en.bioecon.ru/technology/genome-editing/</link><pubDate>Wed, 24 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/genome-editing/</guid><description>Programmable genome editors — CRISPR-Cas9, base editors and prime editors — delivered ex vivo or in vivo via lipid nanoparticles to treat genetic disease, from the first approved CRISPR therapy Casgevy to in-vivo redosable CRISPR and single-dose cardiovascular base editing.</description></item><item><title>Base editing</title><link>https://en.bioecon.ru/technology/base-editing/</link><pubDate>Fri, 19 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/base-editing/</guid><description>Base editors (CBE/ABE) make single-nucleotide changes C·G→T·A and A·T→G·C without double-strand breaks — treating monogenic disease (sickle cell, beta-thalassemia) at up to 90% efficiency with no indels.</description></item><item><title>CRISPR screening as a service</title><link>https://en.bioecon.ru/technology/crispr-screening-as-a-service/</link><pubDate>Fri, 19 Jun 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/crispr-screening-as-a-service/</guid><description>Contract functional-genetic CRISPR screening (pooled sgRNA libraries, lentiviral delivery, NGS) — identifies cancer-resistance genes and drug targets in weeks.</description></item></channel></rss>