Evidence for a New Step in Telomere Maintenance
The strand of telomeric DNA that runs 5′–3′ toward a chromosome end is typically G rich. Telomerase-generated G tails are expected at one end of individual DNA molecules. Saccharomyces telomeres acquire TG 1–3 tails late in S phase. Moreover, the telomeres of linear plasmids can interact when the TG...
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Veröffentlicht in: | Cell 1996-05, Vol.85 (3), p.423-433 |
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description | The strand of telomeric DNA that runs 5′–3′ toward a chromosome end is typically G rich. Telomerase-generated G tails are expected at one end of individual DNA molecules. Saccharomyces telomeres acquire TG
1–3 tails late in S phase. Moreover, the telomeres of linear plasmids can interact when the TG
1–3 tails are present. Molecules that mimic the structures predicted for telomere replication intermediates were generated in vitro. These in vitro generated molecules formed telomere–telomere interactions similar to those on molecules isolated from yeast, but only if both ends that interacted had a TG
1–3 tail. Moreover, TG
1–3 tails were generated in vivo in cells lacking telomerase. These data suggest a new step in telomere maintenance, cell cycle–regulated degradation of the C
1–3A strand, which can generate a potential substrate for telomerase and telomere-binding proteins at every telomere. |
doi_str_mv | 10.1016/S0092-8674(00)81120-4 |
format | Article |
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1–3 tails are present. Molecules that mimic the structures predicted for telomere replication intermediates were generated in vitro. These in vitro generated molecules formed telomere–telomere interactions similar to those on molecules isolated from yeast, but only if both ends that interacted had a TG
1–3 tail. Moreover, TG
1–3 tails were generated in vivo in cells lacking telomerase. These data suggest a new step in telomere maintenance, cell cycle–regulated degradation of the C
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1–3 tails late in S phase. Moreover, the telomeres of linear plasmids can interact when the TG
1–3 tails are present. Molecules that mimic the structures predicted for telomere replication intermediates were generated in vitro. These in vitro generated molecules formed telomere–telomere interactions similar to those on molecules isolated from yeast, but only if both ends that interacted had a TG
1–3 tail. Moreover, TG
1–3 tails were generated in vivo in cells lacking telomerase. These data suggest a new step in telomere maintenance, cell cycle–regulated degradation of the C
1–3A strand, which can generate a potential substrate for telomerase and telomere-binding proteins at every telomere.</description><subject>Base Sequence</subject><subject>Cations - pharmacology</subject><subject>Cell Cycle - genetics</subject><subject>DNA Replication - genetics</subject><subject>DNA, Fungal - genetics</subject><subject>Hot Temperature</subject><subject>Magnesium - pharmacology</subject><subject>Molecular Sequence Data</subject><subject>Plasmids</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>RNA, Fungal - genetics</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - cytology</subject><subject>Saccharomyces cerevisiae - enzymology</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Telomerase - genetics</subject><subject>Telomere - enzymology</subject><subject>Telomere - genetics</subject><issn>0092-8674</issn><issn>1097-4172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EKqXwCZWyQrAIHSdO7KwQqspDKrBoWVuOPZaM8ih2WsTfkz7UbVezuOfOlQ4hYwoPFGg-WQAUSSxyzu4A7gWlCcTsjAwpFDxmlCfnZHhELslVCN8AILIsG5CByGkuCj4kk9nGGWw0Rrb1kYo-8DdadLiKXBMtsWpr9Bi9K9d02KgeuyYXVlUBbw53RL6eZ8vpazz_fHmbPs1jnQHr4qRgXKFKFCSpUKrUwDSnRtsCkxxMqVNmyoJnHArMdJlyi7nVNk0tE2hEkY7I7f7vyrc_awydrF3QWFWqwXYdJBcAPOfpSZByEDmDrAezPah9G4JHK1fe1cr_SQpya1TujMqtLgkgd0Yl63vjw8C6rNEcWweFff64z7HXsXHoZdBua9Q4j7qTpnUnFv4B-VuEHg</recordid><startdate>19960503</startdate><enddate>19960503</enddate><creator>Wellinger, Raymund J</creator><creator>Ethier, Katia</creator><creator>Labrecque, Pascale</creator><creator>Zakian, Virginia A</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><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>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19960503</creationdate><title>Evidence for a New Step in Telomere Maintenance</title><author>Wellinger, Raymund J ; Ethier, Katia ; Labrecque, Pascale ; Zakian, Virginia A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-2947aea2a0238aabc04c71dcf9e260dbc34db975709e5cb37fe6fcf33f48ed893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Base Sequence</topic><topic>Cations - pharmacology</topic><topic>Cell Cycle - genetics</topic><topic>DNA Replication - genetics</topic><topic>DNA, Fungal - genetics</topic><topic>Hot Temperature</topic><topic>Magnesium - pharmacology</topic><topic>Molecular Sequence Data</topic><topic>Plasmids</topic><topic>Repetitive Sequences, Nucleic Acid</topic><topic>RNA, Fungal - genetics</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - cytology</topic><topic>Saccharomyces cerevisiae - enzymology</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Telomerase - genetics</topic><topic>Telomere - enzymology</topic><topic>Telomere - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wellinger, Raymund J</creatorcontrib><creatorcontrib>Ethier, Katia</creatorcontrib><creatorcontrib>Labrecque, Pascale</creatorcontrib><creatorcontrib>Zakian, Virginia A</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wellinger, Raymund J</au><au>Ethier, Katia</au><au>Labrecque, Pascale</au><au>Zakian, Virginia A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence for a New Step in Telomere Maintenance</atitle><jtitle>Cell</jtitle><addtitle>Cell</addtitle><date>1996-05-03</date><risdate>1996</risdate><volume>85</volume><issue>3</issue><spage>423</spage><epage>433</epage><pages>423-433</pages><issn>0092-8674</issn><eissn>1097-4172</eissn><abstract>The strand of telomeric DNA that runs 5′–3′ toward a chromosome end is typically G rich. Telomerase-generated G tails are expected at one end of individual DNA molecules. Saccharomyces telomeres acquire TG
1–3 tails late in S phase. Moreover, the telomeres of linear plasmids can interact when the TG
1–3 tails are present. Molecules that mimic the structures predicted for telomere replication intermediates were generated in vitro. These in vitro generated molecules formed telomere–telomere interactions similar to those on molecules isolated from yeast, but only if both ends that interacted had a TG
1–3 tail. Moreover, TG
1–3 tails were generated in vivo in cells lacking telomerase. These data suggest a new step in telomere maintenance, cell cycle–regulated degradation of the C
1–3A strand, which can generate a potential substrate for telomerase and telomere-binding proteins at every telomere.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>8616897</pmid><doi>10.1016/S0092-8674(00)81120-4</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence Cations - pharmacology Cell Cycle - genetics DNA Replication - genetics DNA, Fungal - genetics Hot Temperature Magnesium - pharmacology Molecular Sequence Data Plasmids Repetitive Sequences, Nucleic Acid RNA, Fungal - genetics Saccharomyces cerevisiae Saccharomyces cerevisiae - cytology Saccharomyces cerevisiae - enzymology Saccharomyces cerevisiae - genetics Telomerase - genetics Telomere - enzymology Telomere - genetics |
title | Evidence for a New Step in Telomere Maintenance |
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