On the Transfer of Information from Old to New Chains of DNA Duplexes in Phage Lambda: Destruction of Heterozygotes
The Watson-Crick model for DNA duplex duplication proposes that the two parental chains separate and that each directs the synthesis of a complementary chain with which it is found associated after the duplication act. Previous experiments have left unchallenged alternative models which propose that...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1970-02, Vol.65 (2), p.363-367 |
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description | The Watson-Crick model for DNA duplex duplication proposes that the two parental chains separate and that each directs the synthesis of a complementary chain with which it is found associated after the duplication act. Previous experiments have left unchallenged alternative models which propose that in any single act of duplication only one of the two parental chains provides information for the synthesis of both new chains. The models are operationally distinguishable since the former demands that heteroduplexes are destroyed by duplication while the latter anticipates their survival. We have shown for phage lambda that duplication destroys heterozygotes as predicted by the Watson-Crick model. A stock of lambda containing a high frequency of heterozygotes at the cI locus was prepared by conducting a cross under conditions of depressed DNA synthesis. Particles in this lysate were permitted to duplicate a few times by adsorbing them to a lambda lysogen in a15N13C medium along with a heteroimmune lambda strain. Emerging lambda particles were separated according to density. The population of particles carrying DNA of parental density retained the initial high heterozygote frequency. Among particles which had duplicated, 80 per cent or more of the heterozygotes had disappeared. |
doi_str_mv | 10.1073/pnas.65.2.363 |
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A stock of lambda containing a high frequency of heterozygotes at the cI locus was prepared by conducting a cross under conditions of depressed DNA synthesis. Particles in this lysate were permitted to duplicate a few times by adsorbing them to a lambda lysogen in a15N13C medium along with a heteroimmune lambda strain. Emerging lambda particles were separated according to density. The population of particles carrying DNA of parental density retained the initial high heterozygote frequency. 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E. A.</creatorcontrib><creatorcontrib>Stahl, Mary M.</creatorcontrib><creatorcontrib>Stahl, Franklin W.</creatorcontrib><title>On the Transfer of Information from Old to New Chains of DNA Duplexes in Phage Lambda: Destruction of Heterozygotes</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The Watson-Crick model for DNA duplex duplication proposes that the two parental chains separate and that each directs the synthesis of a complementary chain with which it is found associated after the duplication act. Previous experiments have left unchallenged alternative models which propose that in any single act of duplication only one of the two parental chains provides information for the synthesis of both new chains. The models are operationally distinguishable since the former demands that heteroduplexes are destroyed by duplication while the latter anticipates their survival. We have shown for phage lambda that duplication destroys heterozygotes as predicted by the Watson-Crick model. A stock of lambda containing a high frequency of heterozygotes at the cI locus was prepared by conducting a cross under conditions of depressed DNA synthesis. Particles in this lysate were permitted to duplicate a few times by adsorbing them to a lambda lysogen in a15N13C medium along with a heteroimmune lambda strain. Emerging lambda particles were separated according to density. The population of particles carrying DNA of parental density retained the initial high heterozygote frequency. Among particles which had duplicated, 80 per cent or more of the heterozygotes had disappeared.</description><subject>Adsorption</subject><subject>Bacteria</subject><subject>Bacteriophage lambda</subject><subject>Bacteriophages</subject><subject>Biochemistry</subject><subject>Biological Sciences: Biochemistry</subject><subject>Carbon Isotopes</subject><subject>Centrifugation</subject><subject>Centrifugation, Density Gradient</subject><subject>Chromosomes</subject><subject>Coliphages - analysis</subject><subject>Coliphages - metabolism</subject><subject>Creeks</subject><subject>DNA Replication</subject><subject>DNA, Viral - biosynthesis</subject><subject>Genetics, Microbial</subject><subject>Heterozygote</subject><subject>Heterozygotes</subject><subject>Modeling</subject><subject>Models, Chemical</subject><subject>Molecules</subject><subject>Polynucleotides - biosynthesis</subject><subject>Virus Replication</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1970</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9v0zAYhi0EGmVw5IJA8gVuKf4Vx0HiMLXAJlUrh3G2nORzmymxO9uBjb8el5YxLpx8eJ73-z7rReglJXNKKv5-50ycy3LO5lzyR2hGSU0LKWryGM0IYVWhBBNP0bMYrwkhdanICTopmeRVRWYorh1OW8BXwbhoIWBv8YWzPowm9d5hG_yI10OHk8eX8AMvtqZ3cW8tL8_wctoNcAsR9w5_3ZoN4JUZm858wEuIKUzt7xlZPocEwf-82_gE8Tl6Ys0Q4cXxPUXfPn-6WpwXq_WXi8XZqmi5lLyoS2F5DYRB2wpWNRaUEI2RpjJVqQxY0rSKCMNBSkpoo0pZdQ0VbVc2JeEdP0UfD3N3UzNC14JLwQx6F_rRhDvtTa__Ja7f6o3_rpliNaU5_-6YD_5myh_SYx9bGAbjwE9R53NUXQuexeIgtsHHGMDe76BE70vS-5K0LDXTuaTsv3l42L19bCXz10e-j_2hD-Jv_4O1nYYhwW3K3quDdx2TD3-31FIo_gvEa68o</recordid><startdate>19700201</startdate><enddate>19700201</enddate><creator>Russo, V. E. A.</creator><creator>Stahl, Mary M.</creator><creator>Stahl, Franklin W.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19700201</creationdate><title>On the Transfer of Information from Old to New Chains of DNA Duplexes in Phage Lambda: Destruction of Heterozygotes</title><author>Russo, V. E. A. ; Stahl, Mary M. ; Stahl, Franklin W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3663-954f39e02ecc427bfe844ba6a7a758aef0bc804a3e66101b8567db14cd5b503d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1970</creationdate><topic>Adsorption</topic><topic>Bacteria</topic><topic>Bacteriophage lambda</topic><topic>Bacteriophages</topic><topic>Biochemistry</topic><topic>Biological Sciences: Biochemistry</topic><topic>Carbon Isotopes</topic><topic>Centrifugation</topic><topic>Centrifugation, Density Gradient</topic><topic>Chromosomes</topic><topic>Coliphages - analysis</topic><topic>Coliphages - metabolism</topic><topic>Creeks</topic><topic>DNA Replication</topic><topic>DNA, Viral - biosynthesis</topic><topic>Genetics, Microbial</topic><topic>Heterozygote</topic><topic>Heterozygotes</topic><topic>Modeling</topic><topic>Models, Chemical</topic><topic>Molecules</topic><topic>Polynucleotides - biosynthesis</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Russo, V. E. A.</creatorcontrib><creatorcontrib>Stahl, Mary M.</creatorcontrib><creatorcontrib>Stahl, Franklin W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Russo, V. E. 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The models are operationally distinguishable since the former demands that heteroduplexes are destroyed by duplication while the latter anticipates their survival. We have shown for phage lambda that duplication destroys heterozygotes as predicted by the Watson-Crick model. A stock of lambda containing a high frequency of heterozygotes at the cI locus was prepared by conducting a cross under conditions of depressed DNA synthesis. Particles in this lysate were permitted to duplicate a few times by adsorbing them to a lambda lysogen in a15N13C medium along with a heteroimmune lambda strain. Emerging lambda particles were separated according to density. The population of particles carrying DNA of parental density retained the initial high heterozygote frequency. Among particles which had duplicated, 80 per cent or more of the heterozygotes had disappeared.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>5263770</pmid><doi>10.1073/pnas.65.2.363</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adsorption Bacteria Bacteriophage lambda Bacteriophages Biochemistry Biological Sciences: Biochemistry Carbon Isotopes Centrifugation Centrifugation, Density Gradient Chromosomes Coliphages - analysis Coliphages - metabolism Creeks DNA Replication DNA, Viral - biosynthesis Genetics, Microbial Heterozygote Heterozygotes Modeling Models, Chemical Molecules Polynucleotides - biosynthesis Virus Replication |
title | On the Transfer of Information from Old to New Chains of DNA Duplexes in Phage Lambda: Destruction of Heterozygotes |
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