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Induction of a Reductive Pathway for Deoxyribonucleotide Synthesis during Early Embryogenesis of the Sea Urchin
Cell-free extracts of Arbacia eggs (Arbacia punctulata) apparently do not contain an enzymatic system for the reduction of ribonucleotides to deoxyribonucleotides. However, during an interval of 5 hr after fertilization at 23 degrees, an enzymatic system is produced that is capable of catalyzing the...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1972-08, Vol.69 (8), p.2006-2010 |
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container_end_page | 2010 |
container_issue | 8 |
container_start_page | 2006 |
container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Noronha, John M. Sheys, Gerald H. Buchanan, John M. |
description | Cell-free extracts of Arbacia eggs (Arbacia punctulata) apparently do not contain an enzymatic system for the reduction of ribonucleotides to deoxyribonucleotides. However, during an interval of 5 hr after fertilization at 23 degrees, an enzymatic system is produced that is capable of catalyzing the reduction of CDP to dCDP in the presence of Mg2+, ethylenediaminetetraacetate, ATP, and a reducing agent, dithiothreitol. The activity is first seen about 1 hr after fertilization, and reaches a peak at about 5 hr. The appearance of the ribonucleotide reductase is prevented by the addition of emetine or puromycin, inhibitors of protein synthesis, to the cells before fertilization. Inclusion of actinomycin D in the cell suspension at a concentration sufficient to inhibit synthesis of messenger RNA does not appreciably affect the production of the enzyme activity. Preexisting, maternal RNA is thus used for synthesis of reductase. Ribonucleotide reductase may, therefore, represent the first example of an enzyme system absent in unfertilized eggs that is produced in response to fertilization. |
doi_str_mv | 10.1073/pnas.69.8.2006 |
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However, during an interval of 5 hr after fertilization at 23 degrees, an enzymatic system is produced that is capable of catalyzing the reduction of CDP to dCDP in the presence of Mg2+, ethylenediaminetetraacetate, ATP, and a reducing agent, dithiothreitol. The activity is first seen about 1 hr after fertilization, and reaches a peak at about 5 hr. The appearance of the ribonucleotide reductase is prevented by the addition of emetine or puromycin, inhibitors of protein synthesis, to the cells before fertilization. Inclusion of actinomycin D in the cell suspension at a concentration sufficient to inhibit synthesis of messenger RNA does not appreciably affect the production of the enzyme activity. Preexisting, maternal RNA is thus used for synthesis of reductase. Ribonucleotide reductase may, therefore, represent the first example of an enzyme system absent in unfertilized eggs that is produced in response to fertilization.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.69.8.2006</identifier><identifier>PMID: 4626400</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Actinomycin ; Adenosine Triphosphate ; Alcohol Oxidoreductases - biosynthesis ; Animals ; Biological Sciences: Biochemistry ; Cell Fractionation ; Cell-Free System ; Centrifugation, Density Gradient ; Chromatography, Ion Exchange ; Cytosine Nucleotides - metabolism ; Dactinomycin - pharmacology ; Deoxyribonucleotides - biosynthesis ; Dithiothreitol ; DNA ; Edetic Acid ; Eggs ; Embryo, Nonmammalian - enzymology ; Embryogenesis ; Embryos ; Emetine - pharmacology ; Enzyme Induction ; Enzymes ; Female ; Fertilization ; Magnesium ; Nucleotides ; Nucleotides - biosynthesis ; Ovum - drug effects ; Proteins - antagonists & inhibitors ; Puromycin - pharmacology ; Ribonucleotides ; RNA ; RNA, Messenger - antagonists & inhibitors ; Sea Urchins - embryology</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1972-08, Vol.69 (8), p.2006-2010</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-54cb0e44d37478f2776a20ffde2a3c4b6f207fcf3504e506573f8bf62d7aed623</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/69/8.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/61461$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/61461$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774,58219,58452</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4626400$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Noronha, John M.</creatorcontrib><creatorcontrib>Sheys, Gerald H.</creatorcontrib><creatorcontrib>Buchanan, John M.</creatorcontrib><title>Induction of a Reductive Pathway for Deoxyribonucleotide Synthesis during Early Embryogenesis of the Sea Urchin</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Cell-free extracts of Arbacia eggs (Arbacia punctulata) apparently do not contain an enzymatic system for the reduction of ribonucleotides to deoxyribonucleotides. However, during an interval of 5 hr after fertilization at 23 degrees, an enzymatic system is produced that is capable of catalyzing the reduction of CDP to dCDP in the presence of Mg2+, ethylenediaminetetraacetate, ATP, and a reducing agent, dithiothreitol. The activity is first seen about 1 hr after fertilization, and reaches a peak at about 5 hr. The appearance of the ribonucleotide reductase is prevented by the addition of emetine or puromycin, inhibitors of protein synthesis, to the cells before fertilization. Inclusion of actinomycin D in the cell suspension at a concentration sufficient to inhibit synthesis of messenger RNA does not appreciably affect the production of the enzyme activity. Preexisting, maternal RNA is thus used for synthesis of reductase. Ribonucleotide reductase may, therefore, represent the first example of an enzyme system absent in unfertilized eggs that is produced in response to fertilization.</description><subject>Actinomycin</subject><subject>Adenosine Triphosphate</subject><subject>Alcohol Oxidoreductases - biosynthesis</subject><subject>Animals</subject><subject>Biological Sciences: Biochemistry</subject><subject>Cell Fractionation</subject><subject>Cell-Free System</subject><subject>Centrifugation, Density Gradient</subject><subject>Chromatography, Ion Exchange</subject><subject>Cytosine Nucleotides - metabolism</subject><subject>Dactinomycin - pharmacology</subject><subject>Deoxyribonucleotides - biosynthesis</subject><subject>Dithiothreitol</subject><subject>DNA</subject><subject>Edetic Acid</subject><subject>Eggs</subject><subject>Embryo, Nonmammalian - enzymology</subject><subject>Embryogenesis</subject><subject>Embryos</subject><subject>Emetine - pharmacology</subject><subject>Enzyme Induction</subject><subject>Enzymes</subject><subject>Female</subject><subject>Fertilization</subject><subject>Magnesium</subject><subject>Nucleotides</subject><subject>Nucleotides - biosynthesis</subject><subject>Ovum - drug effects</subject><subject>Proteins - antagonists & inhibitors</subject><subject>Puromycin - pharmacology</subject><subject>Ribonucleotides</subject><subject>RNA</subject><subject>RNA, Messenger - antagonists & inhibitors</subject><subject>Sea Urchins - embryology</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1972</creationdate><recordtype>article</recordtype><recordid>eNptkcFv0zAYxS0EGmVw5YCE5BO3lC-O4yQHDmgrMGkSiLGz5TifW0-pXWxnLP89yVpKkThZ1vu99z7pEfI6h2UOVfF-51RcimZZLxmAeEIWOTR5JngDT8kCgFVZzRl_Tl7EeAcATVnDGTnjggkOsCD-ynWDTtY76g1V9Ds-fu-RflNp80uN1PhAL9E_jMG23g26R59sh_RmdGmD0UbaDcG6NV2p0I90tW3D6NfoHqUpc4LoDSp6G_TGupfkmVF9xFeH95zcflr9uPiSXX_9fHXx8TrTvBQpK7luATnviopXtWFVJRQDYzpkqtC8FYZBZbQpSuBYgiirwtStEayrFHaCFefkwz53N7Rb7DS6FFQvd8FuVRilV1b-qzi7kWt_LzkTdSkm_7uDP_ifA8YktzZq7Hvl0A9R1nk5dbIZXO5BHXyMAc2xIwc5LyTnhaRoZC3nhSbD29PLjvhhkpPm2fdHPfqlGfo-4UM6CfovOOlv9vpdTD78BXIu8uI33SSwcw</recordid><startdate>19720801</startdate><enddate>19720801</enddate><creator>Noronha, John M.</creator><creator>Sheys, Gerald H.</creator><creator>Buchanan, John M.</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>19720801</creationdate><title>Induction of a Reductive Pathway for Deoxyribonucleotide Synthesis during Early Embryogenesis of the Sea Urchin</title><author>Noronha, John M. ; Sheys, Gerald H. ; Buchanan, John M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-54cb0e44d37478f2776a20ffde2a3c4b6f207fcf3504e506573f8bf62d7aed623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1972</creationdate><topic>Actinomycin</topic><topic>Adenosine Triphosphate</topic><topic>Alcohol Oxidoreductases - biosynthesis</topic><topic>Animals</topic><topic>Biological Sciences: Biochemistry</topic><topic>Cell Fractionation</topic><topic>Cell-Free System</topic><topic>Centrifugation, Density Gradient</topic><topic>Chromatography, Ion Exchange</topic><topic>Cytosine Nucleotides - metabolism</topic><topic>Dactinomycin - pharmacology</topic><topic>Deoxyribonucleotides - biosynthesis</topic><topic>Dithiothreitol</topic><topic>DNA</topic><topic>Edetic Acid</topic><topic>Eggs</topic><topic>Embryo, Nonmammalian - enzymology</topic><topic>Embryogenesis</topic><topic>Embryos</topic><topic>Emetine - pharmacology</topic><topic>Enzyme Induction</topic><topic>Enzymes</topic><topic>Female</topic><topic>Fertilization</topic><topic>Magnesium</topic><topic>Nucleotides</topic><topic>Nucleotides - biosynthesis</topic><topic>Ovum - drug effects</topic><topic>Proteins - antagonists & inhibitors</topic><topic>Puromycin - pharmacology</topic><topic>Ribonucleotides</topic><topic>RNA</topic><topic>RNA, Messenger - antagonists & inhibitors</topic><topic>Sea Urchins - embryology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Noronha, John M.</creatorcontrib><creatorcontrib>Sheys, Gerald H.</creatorcontrib><creatorcontrib>Buchanan, John M.</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>Noronha, John M.</au><au>Sheys, Gerald H.</au><au>Buchanan, John M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of a Reductive Pathway for Deoxyribonucleotide Synthesis during Early Embryogenesis of the Sea Urchin</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1972-08-01</date><risdate>1972</risdate><volume>69</volume><issue>8</issue><spage>2006</spage><epage>2010</epage><pages>2006-2010</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Cell-free extracts of Arbacia eggs (Arbacia punctulata) apparently do not contain an enzymatic system for the reduction of ribonucleotides to deoxyribonucleotides. However, during an interval of 5 hr after fertilization at 23 degrees, an enzymatic system is produced that is capable of catalyzing the reduction of CDP to dCDP in the presence of Mg2+, ethylenediaminetetraacetate, ATP, and a reducing agent, dithiothreitol. The activity is first seen about 1 hr after fertilization, and reaches a peak at about 5 hr. The appearance of the ribonucleotide reductase is prevented by the addition of emetine or puromycin, inhibitors of protein synthesis, to the cells before fertilization. Inclusion of actinomycin D in the cell suspension at a concentration sufficient to inhibit synthesis of messenger RNA does not appreciably affect the production of the enzyme activity. Preexisting, maternal RNA is thus used for synthesis of reductase. Ribonucleotide reductase may, therefore, represent the first example of an enzyme system absent in unfertilized eggs that is produced in response to fertilization.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>4626400</pmid><doi>10.1073/pnas.69.8.2006</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actinomycin Adenosine Triphosphate Alcohol Oxidoreductases - biosynthesis Animals Biological Sciences: Biochemistry Cell Fractionation Cell-Free System Centrifugation, Density Gradient Chromatography, Ion Exchange Cytosine Nucleotides - metabolism Dactinomycin - pharmacology Deoxyribonucleotides - biosynthesis Dithiothreitol DNA Edetic Acid Eggs Embryo, Nonmammalian - enzymology Embryogenesis Embryos Emetine - pharmacology Enzyme Induction Enzymes Female Fertilization Magnesium Nucleotides Nucleotides - biosynthesis Ovum - drug effects Proteins - antagonists & inhibitors Puromycin - pharmacology Ribonucleotides RNA RNA, Messenger - antagonists & inhibitors Sea Urchins - embryology |
title | Induction of a Reductive Pathway for Deoxyribonucleotide Synthesis during Early Embryogenesis of the Sea Urchin |
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