The CCAAT-binding complex of eukaryotes: evolution of a second NLS in the HapB subunit of the filamentous fungus Aspergillus nidulans despite functional conservation at the molecular level between yeast, A.nidulans and human

The heterotrimeric CCAAT-binding complex is evolutionarily conserved in eukaryotic organisms, including fungi, plants and mammals. In the filamentous fungus Aspergillus nidulans, the corresponding complex was designated AnCF (A.nidulans CCAAT-binding factor). AnCF consists of the subunits HapB, HapC...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of molecular biology 2005-09, Vol.352 (3), p.517-533
Hauptverfasser: Tüncher, André, Spröte, Petra, Gehrke, Alexander, Brakhage, Axel A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 533
container_issue 3
container_start_page 517
container_title Journal of molecular biology
container_volume 352
creator Tüncher, André
Spröte, Petra
Gehrke, Alexander
Brakhage, Axel A
description The heterotrimeric CCAAT-binding complex is evolutionarily conserved in eukaryotic organisms, including fungi, plants and mammals. In the filamentous fungus Aspergillus nidulans, the corresponding complex was designated AnCF (A.nidulans CCAAT-binding factor). AnCF consists of the subunits HapB, HapC and HapE. All three subunits are necessary for DNA binding. HapB contains two putative nuclear localisation signal sequences (NLSs) designated NLS1 and NLS2. Previously, it was shown that only NLS2 was required for nuclear localisation of HapB. Furthermore, HapC and HapE are transported to the nucleus only in complex with HapB via a piggy back mechanism. Here, by using various GFP constructs and by establishing a novel marker gene for transformation of A.nidulans, i.e. the pabaA gene encoding p-aminobenzoic acid synthase, it was shown that the HapB homologous proteins of both Saccharomyces cerevisiae (Hap2p) and human (NF-YA) use an NLS homologous to HapB NLS1 for nuclear localisation in S.cerevisiae. Interestingly, for A.nidulans HapB, NLS1 was sufficient for nuclear localisation in S.cerevisiae. In A.nidulans, HapB NLS1 was also functional when present in a different protein context. However, in A.nidulans, both S.cerevisiae Hap2p and human NF-YA entered the nucleus only when HapB NLS2 was present in the respective proteins. In that case, both proteins Hap2p and NF-YA complemented, at least in part, the hap phenotype of A.nidulans with respect to lack of growth on acetamide. Similarly, A.nidulans HapB and human NF-YA complemented a hap2 mutant of S.cerevisiae. In summary, HapB, Hap2p and NF-YA are interchangeable. Because the A.nidulans hapB mutant was complemented, at least in part, by both the human NF-YA and S.cerevisiae Hap2p this finding suggests that the piggy-back mechanism of nuclear transport found for A.nidulans is conserved in yeast and human.
doi_str_mv 10.1016/j.jmb.2005.06.068
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68553789</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68553789</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2414-b2877222ba6cdebf8b7437e088c7f38a13a847e9a12094c25330f6f34b85183e3</originalsourceid><addsrcrecordid>eNqFUcuO1DAQ9AHELgMfwAX5xIkEP_JwuA0jYJFGcGA4R7bTmfXg2CG2B_Zv-RSc3REckVrqlruquqxC6AUlJSW0eXMqT5MqGSF1SZpc4hG6JoSxggneXKGnIZxIXvJKPEFXtCGdyPM1-n24BbzbbbeHQhk3GHfE2k-zhV_YjxjSd7nc-QjhLYaztyka79aFxAG0dwP-vP-KjcMxq9zI-R0OSSVn4opZ30Zj5QQu-hTwmNwxt22YYTkaa_PszJCsdAEPEGYTYcXo9Ya02YYLsJzl_UkZ7-Umb0FnxoItnMFiBfEngMN3IEN8jbflX0GZvd2mSbpn6PEobYDnl75B3z68P-xuiv2Xj592232hWUWrQjHRtowxJRs9gBqFaiveAhFCtyMXknIpqhY6SRnpKs1qzsnYjLxSoqaCA9-gVw-68-J_JAixn0zQYLMbyL_vG1HXvBXdf4G05V3FczobRB-AevEhLDD282KmnEdPSb9m3p_6nHm_Zt6TJpfInJcX8aQmGP4xLoHzP4Xuruc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17394385</pqid></control><display><type>article</type><title>The CCAAT-binding complex of eukaryotes: evolution of a second NLS in the HapB subunit of the filamentous fungus Aspergillus nidulans despite functional conservation at the molecular level between yeast, A.nidulans and human</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Tüncher, André ; Spröte, Petra ; Gehrke, Alexander ; Brakhage, Axel A</creator><creatorcontrib>Tüncher, André ; Spröte, Petra ; Gehrke, Alexander ; Brakhage, Axel A</creatorcontrib><description>The heterotrimeric CCAAT-binding complex is evolutionarily conserved in eukaryotic organisms, including fungi, plants and mammals. In the filamentous fungus Aspergillus nidulans, the corresponding complex was designated AnCF (A.nidulans CCAAT-binding factor). AnCF consists of the subunits HapB, HapC and HapE. All three subunits are necessary for DNA binding. HapB contains two putative nuclear localisation signal sequences (NLSs) designated NLS1 and NLS2. Previously, it was shown that only NLS2 was required for nuclear localisation of HapB. Furthermore, HapC and HapE are transported to the nucleus only in complex with HapB via a piggy back mechanism. Here, by using various GFP constructs and by establishing a novel marker gene for transformation of A.nidulans, i.e. the pabaA gene encoding p-aminobenzoic acid synthase, it was shown that the HapB homologous proteins of both Saccharomyces cerevisiae (Hap2p) and human (NF-YA) use an NLS homologous to HapB NLS1 for nuclear localisation in S.cerevisiae. Interestingly, for A.nidulans HapB, NLS1 was sufficient for nuclear localisation in S.cerevisiae. In A.nidulans, HapB NLS1 was also functional when present in a different protein context. However, in A.nidulans, both S.cerevisiae Hap2p and human NF-YA entered the nucleus only when HapB NLS2 was present in the respective proteins. In that case, both proteins Hap2p and NF-YA complemented, at least in part, the hap phenotype of A.nidulans with respect to lack of growth on acetamide. Similarly, A.nidulans HapB and human NF-YA complemented a hap2 mutant of S.cerevisiae. In summary, HapB, Hap2p and NF-YA are interchangeable. Because the A.nidulans hapB mutant was complemented, at least in part, by both the human NF-YA and S.cerevisiae Hap2p this finding suggests that the piggy-back mechanism of nuclear transport found for A.nidulans is conserved in yeast and human.</description><identifier>ISSN: 0022-2836</identifier><identifier>DOI: 10.1016/j.jmb.2005.06.068</identifier><identifier>PMID: 16098534</identifier><language>eng</language><publisher>England</publisher><subject>Amino Acid Sequence ; Aspergillus nidulans ; Aspergillus nidulans - chemistry ; Aspergillus nidulans - genetics ; Base Sequence ; CCAAT-Binding Factor - chemistry ; CCAAT-Binding Factor - genetics ; CCAAT-Binding Factor - metabolism ; Cell Nucleus - metabolism ; Conserved Sequence ; DNA, Fungal - genetics ; Evolution, Molecular ; Fungal Proteins - chemistry ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; Gene Deletion ; Genes, Fungal ; Genetic Complementation Test ; Green Fluorescent Proteins - chemistry ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Humans ; In Vitro Techniques ; Molecular Sequence Data ; Mutation ; Nuclear Localization Signals - genetics ; Protein Subunits ; Recombinant Fusion Proteins - chemistry ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae Proteins - chemistry ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - metabolism ; Sequence Homology, Amino Acid ; Species Specificity</subject><ispartof>Journal of molecular biology, 2005-09, Vol.352 (3), p.517-533</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2414-b2877222ba6cdebf8b7437e088c7f38a13a847e9a12094c25330f6f34b85183e3</citedby><cites>FETCH-LOGICAL-c2414-b2877222ba6cdebf8b7437e088c7f38a13a847e9a12094c25330f6f34b85183e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16098534$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tüncher, André</creatorcontrib><creatorcontrib>Spröte, Petra</creatorcontrib><creatorcontrib>Gehrke, Alexander</creatorcontrib><creatorcontrib>Brakhage, Axel A</creatorcontrib><title>The CCAAT-binding complex of eukaryotes: evolution of a second NLS in the HapB subunit of the filamentous fungus Aspergillus nidulans despite functional conservation at the molecular level between yeast, A.nidulans and human</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>The heterotrimeric CCAAT-binding complex is evolutionarily conserved in eukaryotic organisms, including fungi, plants and mammals. In the filamentous fungus Aspergillus nidulans, the corresponding complex was designated AnCF (A.nidulans CCAAT-binding factor). AnCF consists of the subunits HapB, HapC and HapE. All three subunits are necessary for DNA binding. HapB contains two putative nuclear localisation signal sequences (NLSs) designated NLS1 and NLS2. Previously, it was shown that only NLS2 was required for nuclear localisation of HapB. Furthermore, HapC and HapE are transported to the nucleus only in complex with HapB via a piggy back mechanism. Here, by using various GFP constructs and by establishing a novel marker gene for transformation of A.nidulans, i.e. the pabaA gene encoding p-aminobenzoic acid synthase, it was shown that the HapB homologous proteins of both Saccharomyces cerevisiae (Hap2p) and human (NF-YA) use an NLS homologous to HapB NLS1 for nuclear localisation in S.cerevisiae. Interestingly, for A.nidulans HapB, NLS1 was sufficient for nuclear localisation in S.cerevisiae. In A.nidulans, HapB NLS1 was also functional when present in a different protein context. However, in A.nidulans, both S.cerevisiae Hap2p and human NF-YA entered the nucleus only when HapB NLS2 was present in the respective proteins. In that case, both proteins Hap2p and NF-YA complemented, at least in part, the hap phenotype of A.nidulans with respect to lack of growth on acetamide. Similarly, A.nidulans HapB and human NF-YA complemented a hap2 mutant of S.cerevisiae. In summary, HapB, Hap2p and NF-YA are interchangeable. Because the A.nidulans hapB mutant was complemented, at least in part, by both the human NF-YA and S.cerevisiae Hap2p this finding suggests that the piggy-back mechanism of nuclear transport found for A.nidulans is conserved in yeast and human.</description><subject>Amino Acid Sequence</subject><subject>Aspergillus nidulans</subject><subject>Aspergillus nidulans - chemistry</subject><subject>Aspergillus nidulans - genetics</subject><subject>Base Sequence</subject><subject>CCAAT-Binding Factor - chemistry</subject><subject>CCAAT-Binding Factor - genetics</subject><subject>CCAAT-Binding Factor - metabolism</subject><subject>Cell Nucleus - metabolism</subject><subject>Conserved Sequence</subject><subject>DNA, Fungal - genetics</subject><subject>Evolution, Molecular</subject><subject>Fungal Proteins - chemistry</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>Gene Deletion</subject><subject>Genes, Fungal</subject><subject>Genetic Complementation Test</subject><subject>Green Fluorescent Proteins - chemistry</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Nuclear Localization Signals - genetics</subject><subject>Protein Subunits</subject><subject>Recombinant Fusion Proteins - chemistry</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae Proteins - chemistry</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><subject>Sequence Homology, Amino Acid</subject><subject>Species Specificity</subject><issn>0022-2836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUcuO1DAQ9AHELgMfwAX5xIkEP_JwuA0jYJFGcGA4R7bTmfXg2CG2B_Zv-RSc3REckVrqlruquqxC6AUlJSW0eXMqT5MqGSF1SZpc4hG6JoSxggneXKGnIZxIXvJKPEFXtCGdyPM1-n24BbzbbbeHQhk3GHfE2k-zhV_YjxjSd7nc-QjhLYaztyka79aFxAG0dwP-vP-KjcMxq9zI-R0OSSVn4opZ30Zj5QQu-hTwmNwxt22YYTkaa_PszJCsdAEPEGYTYcXo9Ya02YYLsJzl_UkZ7-Umb0FnxoItnMFiBfEngMN3IEN8jbflX0GZvd2mSbpn6PEobYDnl75B3z68P-xuiv2Xj592232hWUWrQjHRtowxJRs9gBqFaiveAhFCtyMXknIpqhY6SRnpKs1qzsnYjLxSoqaCA9-gVw-68-J_JAixn0zQYLMbyL_vG1HXvBXdf4G05V3FczobRB-AevEhLDD282KmnEdPSb9m3p_6nHm_Zt6TJpfInJcX8aQmGP4xLoHzP4Xuruc</recordid><startdate>20050923</startdate><enddate>20050923</enddate><creator>Tüncher, André</creator><creator>Spröte, Petra</creator><creator>Gehrke, Alexander</creator><creator>Brakhage, Axel A</creator><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>M7N</scope><scope>7X8</scope></search><sort><creationdate>20050923</creationdate><title>The CCAAT-binding complex of eukaryotes: evolution of a second NLS in the HapB subunit of the filamentous fungus Aspergillus nidulans despite functional conservation at the molecular level between yeast, A.nidulans and human</title><author>Tüncher, André ; Spröte, Petra ; Gehrke, Alexander ; Brakhage, Axel A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2414-b2877222ba6cdebf8b7437e088c7f38a13a847e9a12094c25330f6f34b85183e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Amino Acid Sequence</topic><topic>Aspergillus nidulans</topic><topic>Aspergillus nidulans - chemistry</topic><topic>Aspergillus nidulans - genetics</topic><topic>Base Sequence</topic><topic>CCAAT-Binding Factor - chemistry</topic><topic>CCAAT-Binding Factor - genetics</topic><topic>CCAAT-Binding Factor - metabolism</topic><topic>Cell Nucleus - metabolism</topic><topic>Conserved Sequence</topic><topic>DNA, Fungal - genetics</topic><topic>Evolution, Molecular</topic><topic>Fungal Proteins - chemistry</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - metabolism</topic><topic>Gene Deletion</topic><topic>Genes, Fungal</topic><topic>Genetic Complementation Test</topic><topic>Green Fluorescent Proteins - chemistry</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Nuclear Localization Signals - genetics</topic><topic>Protein Subunits</topic><topic>Recombinant Fusion Proteins - chemistry</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae Proteins - chemistry</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Saccharomyces cerevisiae Proteins - metabolism</topic><topic>Sequence Homology, Amino Acid</topic><topic>Species Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tüncher, André</creatorcontrib><creatorcontrib>Spröte, Petra</creatorcontrib><creatorcontrib>Gehrke, Alexander</creatorcontrib><creatorcontrib>Brakhage, Axel A</creatorcontrib><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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tüncher, André</au><au>Spröte, Petra</au><au>Gehrke, Alexander</au><au>Brakhage, Axel A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The CCAAT-binding complex of eukaryotes: evolution of a second NLS in the HapB subunit of the filamentous fungus Aspergillus nidulans despite functional conservation at the molecular level between yeast, A.nidulans and human</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>2005-09-23</date><risdate>2005</risdate><volume>352</volume><issue>3</issue><spage>517</spage><epage>533</epage><pages>517-533</pages><issn>0022-2836</issn><abstract>The heterotrimeric CCAAT-binding complex is evolutionarily conserved in eukaryotic organisms, including fungi, plants and mammals. In the filamentous fungus Aspergillus nidulans, the corresponding complex was designated AnCF (A.nidulans CCAAT-binding factor). AnCF consists of the subunits HapB, HapC and HapE. All three subunits are necessary for DNA binding. HapB contains two putative nuclear localisation signal sequences (NLSs) designated NLS1 and NLS2. Previously, it was shown that only NLS2 was required for nuclear localisation of HapB. Furthermore, HapC and HapE are transported to the nucleus only in complex with HapB via a piggy back mechanism. Here, by using various GFP constructs and by establishing a novel marker gene for transformation of A.nidulans, i.e. the pabaA gene encoding p-aminobenzoic acid synthase, it was shown that the HapB homologous proteins of both Saccharomyces cerevisiae (Hap2p) and human (NF-YA) use an NLS homologous to HapB NLS1 for nuclear localisation in S.cerevisiae. Interestingly, for A.nidulans HapB, NLS1 was sufficient for nuclear localisation in S.cerevisiae. In A.nidulans, HapB NLS1 was also functional when present in a different protein context. However, in A.nidulans, both S.cerevisiae Hap2p and human NF-YA entered the nucleus only when HapB NLS2 was present in the respective proteins. In that case, both proteins Hap2p and NF-YA complemented, at least in part, the hap phenotype of A.nidulans with respect to lack of growth on acetamide. Similarly, A.nidulans HapB and human NF-YA complemented a hap2 mutant of S.cerevisiae. In summary, HapB, Hap2p and NF-YA are interchangeable. Because the A.nidulans hapB mutant was complemented, at least in part, by both the human NF-YA and S.cerevisiae Hap2p this finding suggests that the piggy-back mechanism of nuclear transport found for A.nidulans is conserved in yeast and human.</abstract><cop>England</cop><pmid>16098534</pmid><doi>10.1016/j.jmb.2005.06.068</doi><tpages>17</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-2836
ispartof Journal of molecular biology, 2005-09, Vol.352 (3), p.517-533
issn 0022-2836
language eng
recordid cdi_proquest_miscellaneous_68553789
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Amino Acid Sequence
Aspergillus nidulans
Aspergillus nidulans - chemistry
Aspergillus nidulans - genetics
Base Sequence
CCAAT-Binding Factor - chemistry
CCAAT-Binding Factor - genetics
CCAAT-Binding Factor - metabolism
Cell Nucleus - metabolism
Conserved Sequence
DNA, Fungal - genetics
Evolution, Molecular
Fungal Proteins - chemistry
Fungal Proteins - genetics
Fungal Proteins - metabolism
Gene Deletion
Genes, Fungal
Genetic Complementation Test
Green Fluorescent Proteins - chemistry
Green Fluorescent Proteins - genetics
Green Fluorescent Proteins - metabolism
Humans
In Vitro Techniques
Molecular Sequence Data
Mutation
Nuclear Localization Signals - genetics
Protein Subunits
Recombinant Fusion Proteins - chemistry
Recombinant Fusion Proteins - genetics
Recombinant Fusion Proteins - metabolism
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins - chemistry
Saccharomyces cerevisiae Proteins - genetics
Saccharomyces cerevisiae Proteins - metabolism
Sequence Homology, Amino Acid
Species Specificity
title The CCAAT-binding complex of eukaryotes: evolution of a second NLS in the HapB subunit of the filamentous fungus Aspergillus nidulans despite functional conservation at the molecular level between yeast, A.nidulans and human
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T09%3A46%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20CCAAT-binding%20complex%20of%20eukaryotes:%20evolution%20of%20a%20second%20NLS%20in%20the%20HapB%20subunit%20of%20the%20filamentous%20fungus%20Aspergillus%20nidulans%20despite%20functional%20conservation%20at%20the%20molecular%20level%20between%20yeast,%20A.nidulans%20and%20human&rft.jtitle=Journal%20of%20molecular%20biology&rft.au=T%C3%BCncher,%20Andr%C3%A9&rft.date=2005-09-23&rft.volume=352&rft.issue=3&rft.spage=517&rft.epage=533&rft.pages=517-533&rft.issn=0022-2836&rft_id=info:doi/10.1016/j.jmb.2005.06.068&rft_dat=%3Cproquest_cross%3E68553789%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17394385&rft_id=info:pmid/16098534&rfr_iscdi=true