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Path: ...!2.eu.feeder.erje.net!feeder.erje.net!feeds.news.ox.ac.uk!news.ox.ac.uk!nntp-feed.chiark.greenend.org.uk!ewrotcd!news.killfile.org!news.eyrie.org!beagle.ediacara.org!.POSTED.beagle.ediacara.org!not-for-mail From: RonO <rokimoto557@gmail.com> Newsgroups: talk.origins Subject: Transposase evolved to insert DNA at specific locations Date: Sat, 17 May 2025 10:53:44 -0500 Organization: A noiseless patient Spider Lines: 17 Sender: to%beagle.ediacara.org Approved: moderator@beagle.ediacara.org Message-ID: <100abe8$f58t$1@dont-email.me> Reply-To: rokimoto557@gmail.com MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; format=flowed Content-Transfer-Encoding: 7bit Injection-Info: beagle.ediacara.org; posting-host="beagle.ediacara.org:3.132.105.89"; logging-data="37130"; mail-complaints-to="usenet@beagle.ediacara.org" User-Agent: Mozilla Thunderbird To: talk-origins@moderators.isc.org Cancel-Lock: sha1:ySy8L6OptmKBD2On/d2jSr9thpY= Return-Path: <news@eternal-september.org> X-Original-To: talk-origins@ediacara.org Delivered-To: talk-origins@ediacara.org id 8945B22978C; Sat, 17 May 2025 11:53:50 -0400 (EDT) by beagle.ediacara.org (Postfix) with ESMTPS id 59B90229783 for <talk-origins@ediacara.org>; Sat, 17 May 2025 11:53:48 -0400 (EDT) id 1C46D1C04DE; Sat, 17 May 2025 15:53:47 +0000 (UTC) Delivered-To: talk-origins@moderators.isc.org by newsfeed.bofh.team (Postfix) with ESMTPS id 0BA991C00B6 for <talk-origins@moderators.isc.org>; Sat, 17 May 2025 15:53:47 +0000 (UTC) (using TLSv1.3 with cipher TLS_AES_256_GCM_SHA384 (256/256 bits) key-exchange X25519 server-signature ECDSA (P-256)) (No client certificate requested) by smtp.eternal-september.org (Postfix) with ESMTPS id 250DB60A01 for <talk-origins@moderators.isc.org>; Sat, 17 May 2025 15:53:45 +0000 (UTC) Authentication-Results: name/250DB60A01; dmarc=fail (p=none dis=none) header.from=gmail.com id CA1DCDC01CA; Sat, 17 May 2025 17:53:44 +0200 (CEST) X-Injection-Date: Sat, 17 May 2025 17:53:44 +0200 (CEST) X-Auth-Sender: U2FsdGVkX183ZHL0e7or70CR09Xj1HRhsjRq27GDO/M= Content-Language: en-US DKIM_ADSP_CUSTOM_MED,FORGED_GMAIL_RCVD,FREEMAIL_FORGED_REPLYTO, FREEMAIL_REPLYTO_END_DIGIT,HEADER_FROM_DIFFERENT_DOMAINS, NML_ADSP_CUSTOM_MED,RCVD_IN_DNSWL_BLOCKED, RCVD_IN_VALIDITY_RPBL_BLOCKED,RCVD_IN_VALIDITY_SAFE_BLOCKED, RCVD_IN_ZEN_BLOCKED_OPENDNS,SPF_HELO_NONE,SPF_PASS,URIBL_BLOCKED, URIBL_DBL_BLOCKED_OPENDNS,URIBL_ZEN_BLOCKED_OPENDNS, USER_IN_WELCOMELIST,USER_IN_WHITELIST autolearn=ham autolearn_force=no version=3.4.6 smtp.eternal-september.org Bytes: 3712 https://www.science.org/content/article/jumping-gene-enzyme-can-make-big-precise-changes-human-dna An enzyme usually used by bacterial transposons to move from one place to another in the bacterial genome has been modified and evolved to insert large pieces of DNA into specific locations in mammalian genomes. It uses the guide RNA of CRISPR to identify specific genomic sequence and they evolved the enzyme in order to improve the rate that it would insert sequence at the guide RNA location. They used an in vivo selection environment where bacteria with the the enzyme had to survive viral infection. They could survive viral infection if the enzyme could perform specific functions in the bacterial cell, so random mutations in the enzyme were selected for improved ability to perform the required duties. They ended up with an enzyme that was much better than what they started with, and it could be useful for inserting large gene length segments of DNA into the human genome for fixing genetic defects. Ron Okimoto