Complete DNA sequence of yeast chromosome II
In the framework of the EU genome-sequencing programmes, the complete DNA sequence of the yeast Saccharomyces cerevisiae chromosome II (807 188 bp) has been determined. At present, this is the largest eukaryotic chromosome entirely sequenced. A total of 410 open reading frames (ORFs) were identified...
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Veröffentlicht in: | The EMBO journal 1994-12, Vol.13 (24), p.5795-5809 |
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description | In the framework of the EU genome-sequencing programmes, the complete DNA sequence of the yeast Saccharomyces cerevisiae chromosome II (807 188 bp) has been determined. At present, this is the largest eukaryotic chromosome entirely sequenced. A total of 410 open reading frames (ORFs) were identified, covering 72% of the sequence. Similarity searches revealed that 124 ORFs (30%) correspond to genes of known function, 51 ORFs (12.5%) appear to be homologues of genes whose functions are known, 52 others (12.5%) have homologues the functions of which are not well defined and another 33 of the novel putative genes (8%) exhibit a degree of similarity which is insufficient to confidently assign function. Of the genes on chromosome II, 37-45% are thus of unpredicted function. Among the novel putative genes, we found several that are related to genes that perform differentiated functions in multicellular organisms or are involved in malignancy. In addition to a compact arrangement of potential protein coding sequences, the analysis of this chromosome confirmed general chromosome patterns but also revealed particular novel features of chromosomal organization. Alternating regional variations in average base composition correlate with variations in local gene density along chromosome II, as observed in chromosomes XI and III. We propose that functional ARS elements are preferably of approximately 110 kb. Similarly, the 13 tRNA genes and the three Ty elements of chromosome II are found in AT-rich regions. In chromosome II, the distribution of coding sequences between the two strands in biased, with a ratio of 1.3.1. An interesting aspect regarding the evolution of the eukaryotic genome is the finding that redundancy, amounting to 16% of the coding capacity. |
doi_str_mv | 10.1002/j.1460-2075.1994.tb06923.x |
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At present, this is the largest eukaryotic chromosome entirely sequenced. A total of 410 open reading frames (ORFs) were identified, covering 72% of the sequence. Similarity searches revealed that 124 ORFs (30%) correspond to genes of known function, 51 ORFs (12.5%) appear to be homologues of genes whose functions are known, 52 others (12.5%) have homologues the functions of which are not well defined and another 33 of the novel putative genes (8%) exhibit a degree of similarity which is insufficient to confidently assign function. Of the genes on chromosome II, 37-45% are thus of unpredicted function. Among the novel putative genes, we found several that are related to genes that perform differentiated functions in multicellular organisms or are involved in malignancy. In addition to a compact arrangement of potential protein coding sequences, the analysis of this chromosome confirmed general chromosome patterns but also revealed particular novel features of chromosomal organization. Alternating regional variations in average base composition correlate with variations in local gene density along chromosome II, as observed in chromosomes XI and III. We propose that functional ARS elements are preferably of approximately 110 kb. Similarly, the 13 tRNA genes and the three Ty elements of chromosome II are found in AT-rich regions. In chromosome II, the distribution of coding sequences between the two strands in biased, with a ratio of 1.3.1. An interesting aspect regarding the evolution of the eukaryotic genome is the finding that redundancy, amounting to 16% of the coding capacity.</description><identifier>ISSN: 0261-4189</identifier><identifier>EISSN: 1460-2075</identifier><identifier>DOI: 10.1002/j.1460-2075.1994.tb06923.x</identifier><identifier>PMID: 7813418</identifier><language>eng</language><publisher>England</publisher><subject>amino acid sequences ; Base Composition ; Base Sequence ; chromosome mapping ; Chromosome Mapping - methods ; chromosomes ; Chromosomes, Fungal - genetics ; Cloning, Molecular ; Cosmids - genetics ; DNA, Fungal - genetics ; gene density ; Genes, Fungal - genetics ; Molecular Sequence Data ; nucleotide sequences ; Open Reading Frames ; proteins ; Quality Control ; Repetitive Sequences, Nucleic Acid ; Reproducibility of Results ; retrotransposons ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Sequence Analysis, DNA ; Sequence Homology, Amino Acid ; structural genes ; Telomere - genetics</subject><ispartof>The EMBO journal, 1994-12, Vol.13 (24), p.5795-5809</ispartof><rights>1994 European Molecular Biology Organization</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5333-c31664ebb6cf295042fa3353a64e45de0e36c9a743635e2df23ee3ffa32a76393</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC395553/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC395553/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7813418$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feldmann, H</creatorcontrib><creatorcontrib>Aigle, M</creatorcontrib><creatorcontrib>Aljinovic, G</creatorcontrib><creatorcontrib>Andre, B</creatorcontrib><creatorcontrib>Baclet, M.C</creatorcontrib><creatorcontrib>Barthe, C</creatorcontrib><creatorcontrib>Baur, A</creatorcontrib><creatorcontrib>Becam, A.M</creatorcontrib><creatorcontrib>Biteau, N</creatorcontrib><creatorcontrib>Boles, E</creatorcontrib><title>Complete DNA sequence of yeast chromosome II</title><title>The EMBO journal</title><addtitle>EMBO J</addtitle><description>In the framework of the EU genome-sequencing programmes, the complete DNA sequence of the yeast Saccharomyces cerevisiae chromosome II (807 188 bp) has been determined. At present, this is the largest eukaryotic chromosome entirely sequenced. A total of 410 open reading frames (ORFs) were identified, covering 72% of the sequence. Similarity searches revealed that 124 ORFs (30%) correspond to genes of known function, 51 ORFs (12.5%) appear to be homologues of genes whose functions are known, 52 others (12.5%) have homologues the functions of which are not well defined and another 33 of the novel putative genes (8%) exhibit a degree of similarity which is insufficient to confidently assign function. Of the genes on chromosome II, 37-45% are thus of unpredicted function. Among the novel putative genes, we found several that are related to genes that perform differentiated functions in multicellular organisms or are involved in malignancy. In addition to a compact arrangement of potential protein coding sequences, the analysis of this chromosome confirmed general chromosome patterns but also revealed particular novel features of chromosomal organization. Alternating regional variations in average base composition correlate with variations in local gene density along chromosome II, as observed in chromosomes XI and III. We propose that functional ARS elements are preferably of approximately 110 kb. Similarly, the 13 tRNA genes and the three Ty elements of chromosome II are found in AT-rich regions. In chromosome II, the distribution of coding sequences between the two strands in biased, with a ratio of 1.3.1. An interesting aspect regarding the evolution of the eukaryotic genome is the finding that redundancy, amounting to 16% of the coding capacity.</description><subject>amino acid sequences</subject><subject>Base Composition</subject><subject>Base Sequence</subject><subject>chromosome mapping</subject><subject>Chromosome Mapping - methods</subject><subject>chromosomes</subject><subject>Chromosomes, Fungal - genetics</subject><subject>Cloning, Molecular</subject><subject>Cosmids - genetics</subject><subject>DNA, Fungal - genetics</subject><subject>gene density</subject><subject>Genes, Fungal - genetics</subject><subject>Molecular Sequence Data</subject><subject>nucleotide sequences</subject><subject>Open Reading Frames</subject><subject>proteins</subject><subject>Quality Control</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>Reproducibility of Results</subject><subject>retrotransposons</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology, Amino Acid</subject><subject>structural genes</subject><subject>Telomere - genetics</subject><issn>0261-4189</issn><issn>1460-2075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUU1vEzEUtBCoTQM_AXXFgVN3sf38ka3UQ0hbCCpwgJ6fHOdtu9FuHNYb2vz7OiSK4FRxsvVm3ujNDGPvBC8E5_LDohDK8FxyqwtRlqroZ9yUEorHF2xwgF6yAZdG5EqMymN2EuOCc65HVhyxIzsSkOYDdjYJ7aqhnrLLb-Ms0q81LT1loco25GKf-fsutCGGlrLp9DV7Vbkm0pv9O2S311c_J5_zm--fppPxTe41AOQehDGKZjPjK1lqrmTlADS4NFR6TpzA-NJZBQY0yXklgQiqRJLOGihhyC52uqv1rKW5p2XfuQZXXd26boPB1fgvsqzv8S78Rii1TicM2fv9fheSodhjW0dPTeOWFNYRbQrLWK2eJSYfVoLSiXi-I_ouxNhRdThGcNx2ggvcBo_b4HHbCe47wce0_PZvO4fVfQkJH-_wh7qhzX8o49XXj1_-_JPG6U6jcgHdXVdHvP0huQAuNOfWangC4sWlMw</recordid><startdate>19941215</startdate><enddate>19941215</enddate><creator>Feldmann, H</creator><creator>Aigle, M</creator><creator>Aljinovic, G</creator><creator>Andre, B</creator><creator>Baclet, M.C</creator><creator>Barthe, C</creator><creator>Baur, A</creator><creator>Becam, A.M</creator><creator>Biteau, N</creator><creator>Boles, E</creator><scope>FBQ</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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19941215</creationdate><title>Complete DNA sequence of yeast chromosome II</title><author>Feldmann, H ; Aigle, M ; Aljinovic, G ; Andre, B ; Baclet, M.C ; Barthe, C ; Baur, A ; Becam, A.M ; Biteau, N ; Boles, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5333-c31664ebb6cf295042fa3353a64e45de0e36c9a743635e2df23ee3ffa32a76393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>amino acid sequences</topic><topic>Base Composition</topic><topic>Base Sequence</topic><topic>chromosome mapping</topic><topic>Chromosome Mapping - methods</topic><topic>chromosomes</topic><topic>Chromosomes, Fungal - genetics</topic><topic>Cloning, Molecular</topic><topic>Cosmids - genetics</topic><topic>DNA, Fungal - genetics</topic><topic>gene density</topic><topic>Genes, Fungal - genetics</topic><topic>Molecular Sequence Data</topic><topic>nucleotide sequences</topic><topic>Open Reading Frames</topic><topic>proteins</topic><topic>Quality Control</topic><topic>Repetitive Sequences, Nucleic Acid</topic><topic>Reproducibility of Results</topic><topic>retrotransposons</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Amino Acid</topic><topic>structural genes</topic><topic>Telomere - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feldmann, H</creatorcontrib><creatorcontrib>Aigle, M</creatorcontrib><creatorcontrib>Aljinovic, G</creatorcontrib><creatorcontrib>Andre, B</creatorcontrib><creatorcontrib>Baclet, M.C</creatorcontrib><creatorcontrib>Barthe, C</creatorcontrib><creatorcontrib>Baur, A</creatorcontrib><creatorcontrib>Becam, A.M</creatorcontrib><creatorcontrib>Biteau, N</creatorcontrib><creatorcontrib>Boles, E</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The EMBO journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feldmann, H</au><au>Aigle, M</au><au>Aljinovic, G</au><au>Andre, B</au><au>Baclet, M.C</au><au>Barthe, C</au><au>Baur, A</au><au>Becam, A.M</au><au>Biteau, N</au><au>Boles, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complete DNA sequence of yeast chromosome II</atitle><jtitle>The EMBO journal</jtitle><addtitle>EMBO J</addtitle><date>1994-12-15</date><risdate>1994</risdate><volume>13</volume><issue>24</issue><spage>5795</spage><epage>5809</epage><pages>5795-5809</pages><issn>0261-4189</issn><eissn>1460-2075</eissn><abstract>In the framework of the EU genome-sequencing programmes, the complete DNA sequence of the yeast Saccharomyces cerevisiae chromosome II (807 188 bp) has been determined. At present, this is the largest eukaryotic chromosome entirely sequenced. A total of 410 open reading frames (ORFs) were identified, covering 72% of the sequence. Similarity searches revealed that 124 ORFs (30%) correspond to genes of known function, 51 ORFs (12.5%) appear to be homologues of genes whose functions are known, 52 others (12.5%) have homologues the functions of which are not well defined and another 33 of the novel putative genes (8%) exhibit a degree of similarity which is insufficient to confidently assign function. Of the genes on chromosome II, 37-45% are thus of unpredicted function. Among the novel putative genes, we found several that are related to genes that perform differentiated functions in multicellular organisms or are involved in malignancy. In addition to a compact arrangement of potential protein coding sequences, the analysis of this chromosome confirmed general chromosome patterns but also revealed particular novel features of chromosomal organization. Alternating regional variations in average base composition correlate with variations in local gene density along chromosome II, as observed in chromosomes XI and III. We propose that functional ARS elements are preferably of approximately 110 kb. Similarly, the 13 tRNA genes and the three Ty elements of chromosome II are found in AT-rich regions. In chromosome II, the distribution of coding sequences between the two strands in biased, with a ratio of 1.3.1. An interesting aspect regarding the evolution of the eukaryotic genome is the finding that redundancy, amounting to 16% of the coding capacity.</abstract><cop>England</cop><pmid>7813418</pmid><doi>10.1002/j.1460-2075.1994.tb06923.x</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | amino acid sequences Base Composition Base Sequence chromosome mapping Chromosome Mapping - methods chromosomes Chromosomes, Fungal - genetics Cloning, Molecular Cosmids - genetics DNA, Fungal - genetics gene density Genes, Fungal - genetics Molecular Sequence Data nucleotide sequences Open Reading Frames proteins Quality Control Repetitive Sequences, Nucleic Acid Reproducibility of Results retrotransposons Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Sequence Analysis, DNA Sequence Homology, Amino Acid structural genes Telomere - genetics |
title | Complete DNA sequence of yeast chromosome II |
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