Relay-Version: version B 2.10 5/3/83; site utzoo.UUCP Path: utzoo!utgpu!water!watnot!watmath!clyde!rutgers!husc6!linus!philabs!aecom!diaz From: diaz@aecom.UUCP Newsgroups: sci.bio Subject: Re: information content of DNA Message-ID: <1010@aecom.UUCP> Date: Sat, 4-Apr-87 22:01:24 EST Article-I.D.: aecom.1010 Posted: Sat Apr 4 22:01:24 1987 Date-Received: Wed, 8-Apr-87 03:31:18 EST References: <2840@ecsvax.UUCP> <11189@teknowledge-vaxc.ARPA> <978@aecom.UUCP> <425@haddock.UUCP> Organization: Graduate School of Hard Knocks Lines: 27 Summary: On multiple reading frames in DNA In article <425@haddock.UUCP>, johnc@haddock.UUCP (John Chambers) writes: > One observation I haven't seen yet is the peculiarity of DNA called "reading > frames" This effectively triples the number of amino-acid sequences a given > chunk of DNA encodes. Multiply this by two for the complementary strand. > > Granted, it is very rare that all six readings actually code for something > in real life. But this doesn't have much to do with the information content. > Forget rare, there ain't no such animal. Although multiple reading frames have been observed in phage, and transcription from complementary strands observed in a variety of organisms (most recently, mice) there is no documented example of anywhere near the six possible readings coding for functional polypeptides. The implications for molecular evolution for such a scheme would be disastrous. Organisms apparently think little about the advantages of compact genomes, prokaryotes included. Rather there seems to be something about having a lot of "junk" DNA that's beneficial, if I may be allowed this ounce of teleology. Granted, we may one day realize that much satellite and intron DNA may have functions we don't even dream about today, but I truly doubt that coding for proteins will be one of them. -- dn/dx = Dan Diaz (philabs!aecom!diaz) Department of Molecular Biology & Pizza Chemistry AECOM "Hold the E.coli"