Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome

Pulmonary surfactant, a lipoprotein complex, is essential for normal lung function, and deficiency of surfactant can result in respiratory-distress syndrome (RDS) in the prematurely born infant. Some studies have pointed towards a genetic contribution to the aetiology of RDS. Because the surfactant...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochemical journal 1995-01, Vol.305 ( Pt 2) (2), p.583-590
Hauptverfasser: Floros, J, Veletza, S V, Kotikalapudi, P, Krizkova, L, Karinch, A M, Friedman, C, Buchter, S, Marks, K
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 590
container_issue 2
container_start_page 583
container_title Biochemical journal
container_volume 305 ( Pt 2)
creator Floros, J
Veletza, S V
Kotikalapudi, P
Krizkova, L
Karinch, A M
Friedman, C
Buchter, S
Marks, K
description Pulmonary surfactant, a lipoprotein complex, is essential for normal lung function, and deficiency of surfactant can result in respiratory-distress syndrome (RDS) in the prematurely born infant. Some studies have pointed towards a genetic contribution to the aetiology of RDS. Because the surfactant protein B (SP-B) is important for optimal surfactant function and because it is involved in the pathogenesis of pulmonary disease, we investigated the genetic variability of the SP-B gene in individuals with and without RDS. We identified a 2.5 kb BamHI polymorphism and studied its location, nature and frequency. We localized this polymorphism in the first half of intron 4 and found that it is derived by gain or loss in the number of copies of a motif that consists of two elements, a 20 bp conserved sequence and a variable number of CA dinucleotides. Variability in the number of motifs resulting from either deletion (in 55.3% of the cases with the variation) or insertion (44.7%) of motifs was observed in genomic DNAs from unrelated individuals. Analysis of 219 genomic DNAs from infants with (n = 82) and without (n = 137) RDS showed that this insertion/deletion appears with significantly higher frequency in the RDS population (29.3 as against 16.8%, P < 0.05).
doi_str_mv 10.1042/bj3050583
format Article
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1136402</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>7832777</sourcerecordid><originalsourceid>FETCH-LOGICAL-c370t-3ebe7b1facef027092019e5a25e6d31d8371f592bc10dc1f991f62ea461c24903</originalsourceid><addsrcrecordid>eNpVkF9LwzAUxYMoc04f_ABCXn2o3iRt074IOv_CwBd9lJImt1vGmpYkFfbtrWwMfboc7jm_A4eQSwY3DFJ-W68FZJAV4ohMWSohKSQvjskUeJ4mOXB2Ss5CWAOwFFKYkIksBJdSTsnXo3WD3mAXrUHqsUcVA7WOxhXS1dAqR8PgG6WjcpH2votoXfJAl-iQKmfGSOitV7Hz28TYEEcdaNg647sWz8lJozYBL_Z3Rj6fnz7mr8ni_eVtfr9ItJAQE4E1ypqNLdgAl1ByYCVmimeYG8FMISRrspLXmoHRrClL1uQcVZozzdMSxIzc7bj9ULdoNLro1abqvW2V31adstX_j7Oratl9V4yJPAU-Aq53AO27EDw2hyyD6nfi6jDx6L36W3Zw7jcVP14CeXk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Floros, J ; Veletza, S V ; Kotikalapudi, P ; Krizkova, L ; Karinch, A M ; Friedman, C ; Buchter, S ; Marks, K</creator><creatorcontrib>Floros, J ; Veletza, S V ; Kotikalapudi, P ; Krizkova, L ; Karinch, A M ; Friedman, C ; Buchter, S ; Marks, K</creatorcontrib><description>Pulmonary surfactant, a lipoprotein complex, is essential for normal lung function, and deficiency of surfactant can result in respiratory-distress syndrome (RDS) in the prematurely born infant. Some studies have pointed towards a genetic contribution to the aetiology of RDS. Because the surfactant protein B (SP-B) is important for optimal surfactant function and because it is involved in the pathogenesis of pulmonary disease, we investigated the genetic variability of the SP-B gene in individuals with and without RDS. We identified a 2.5 kb BamHI polymorphism and studied its location, nature and frequency. We localized this polymorphism in the first half of intron 4 and found that it is derived by gain or loss in the number of copies of a motif that consists of two elements, a 20 bp conserved sequence and a variable number of CA dinucleotides. Variability in the number of motifs resulting from either deletion (in 55.3% of the cases with the variation) or insertion (44.7%) of motifs was observed in genomic DNAs from unrelated individuals. Analysis of 219 genomic DNAs from infants with (n = 82) and without (n = 137) RDS showed that this insertion/deletion appears with significantly higher frequency in the RDS population (29.3 as against 16.8%, P &lt; 0.05).</description><identifier>ISSN: 0264-6021</identifier><identifier>EISSN: 1470-8728</identifier><identifier>DOI: 10.1042/bj3050583</identifier><identifier>PMID: 7832777</identifier><language>eng</language><publisher>England</publisher><subject>African Continental Ancestry Group ; Base Sequence ; Cloning, Molecular ; Deoxyribonuclease BamHI ; European Continental Ancestry Group ; Gene Frequency ; Genetic Variation ; Genome, Human ; Humans ; Infant ; Infant, Newborn ; Introns - genetics ; Molecular Sequence Data ; Mutagenesis, Insertional ; Polymerase Chain Reaction ; Polymorphism, Restriction Fragment Length ; Proteolipids - genetics ; Pulmonary Surfactants - deficiency ; Pulmonary Surfactants - genetics ; Repetitive Sequences, Nucleic Acid - genetics ; Respiratory Distress Syndrome, Newborn - genetics ; Sequence Analysis, DNA ; Sequence Deletion ; Sequence Homology, Nucleic Acid</subject><ispartof>Biochemical journal, 1995-01, Vol.305 ( Pt 2) (2), p.583-590</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-3ebe7b1facef027092019e5a25e6d31d8371f592bc10dc1f991f62ea461c24903</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/PMC1136402/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1136402/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7832777$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Floros, J</creatorcontrib><creatorcontrib>Veletza, S V</creatorcontrib><creatorcontrib>Kotikalapudi, P</creatorcontrib><creatorcontrib>Krizkova, L</creatorcontrib><creatorcontrib>Karinch, A M</creatorcontrib><creatorcontrib>Friedman, C</creatorcontrib><creatorcontrib>Buchter, S</creatorcontrib><creatorcontrib>Marks, K</creatorcontrib><title>Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome</title><title>Biochemical journal</title><addtitle>Biochem J</addtitle><description>Pulmonary surfactant, a lipoprotein complex, is essential for normal lung function, and deficiency of surfactant can result in respiratory-distress syndrome (RDS) in the prematurely born infant. Some studies have pointed towards a genetic contribution to the aetiology of RDS. Because the surfactant protein B (SP-B) is important for optimal surfactant function and because it is involved in the pathogenesis of pulmonary disease, we investigated the genetic variability of the SP-B gene in individuals with and without RDS. We identified a 2.5 kb BamHI polymorphism and studied its location, nature and frequency. We localized this polymorphism in the first half of intron 4 and found that it is derived by gain or loss in the number of copies of a motif that consists of two elements, a 20 bp conserved sequence and a variable number of CA dinucleotides. Variability in the number of motifs resulting from either deletion (in 55.3% of the cases with the variation) or insertion (44.7%) of motifs was observed in genomic DNAs from unrelated individuals. Analysis of 219 genomic DNAs from infants with (n = 82) and without (n = 137) RDS showed that this insertion/deletion appears with significantly higher frequency in the RDS population (29.3 as against 16.8%, P &lt; 0.05).</description><subject>African Continental Ancestry Group</subject><subject>Base Sequence</subject><subject>Cloning, Molecular</subject><subject>Deoxyribonuclease BamHI</subject><subject>European Continental Ancestry Group</subject><subject>Gene Frequency</subject><subject>Genetic Variation</subject><subject>Genome, Human</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Introns - genetics</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis, Insertional</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Proteolipids - genetics</subject><subject>Pulmonary Surfactants - deficiency</subject><subject>Pulmonary Surfactants - genetics</subject><subject>Repetitive Sequences, Nucleic Acid - genetics</subject><subject>Respiratory Distress Syndrome, Newborn - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Deletion</subject><subject>Sequence Homology, Nucleic Acid</subject><issn>0264-6021</issn><issn>1470-8728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkF9LwzAUxYMoc04f_ABCXn2o3iRt074IOv_CwBd9lJImt1vGmpYkFfbtrWwMfboc7jm_A4eQSwY3DFJ-W68FZJAV4ohMWSohKSQvjskUeJ4mOXB2Ss5CWAOwFFKYkIksBJdSTsnXo3WD3mAXrUHqsUcVA7WOxhXS1dAqR8PgG6WjcpH2votoXfJAl-iQKmfGSOitV7Hz28TYEEcdaNg647sWz8lJozYBL_Z3Rj6fnz7mr8ni_eVtfr9ItJAQE4E1ypqNLdgAl1ByYCVmimeYG8FMISRrspLXmoHRrClL1uQcVZozzdMSxIzc7bj9ULdoNLro1abqvW2V31adstX_j7Oratl9V4yJPAU-Aq53AO27EDw2hyyD6nfi6jDx6L36W3Zw7jcVP14CeXk</recordid><startdate>19950115</startdate><enddate>19950115</enddate><creator>Floros, J</creator><creator>Veletza, S V</creator><creator>Kotikalapudi, P</creator><creator>Krizkova, L</creator><creator>Karinch, A M</creator><creator>Friedman, C</creator><creator>Buchter, S</creator><creator>Marks, K</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>5PM</scope></search><sort><creationdate>19950115</creationdate><title>Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome</title><author>Floros, J ; Veletza, S V ; Kotikalapudi, P ; Krizkova, L ; Karinch, A M ; Friedman, C ; Buchter, S ; Marks, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-3ebe7b1facef027092019e5a25e6d31d8371f592bc10dc1f991f62ea461c24903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>African Continental Ancestry Group</topic><topic>Base Sequence</topic><topic>Cloning, Molecular</topic><topic>Deoxyribonuclease BamHI</topic><topic>European Continental Ancestry Group</topic><topic>Gene Frequency</topic><topic>Genetic Variation</topic><topic>Genome, Human</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Introns - genetics</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis, Insertional</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Proteolipids - genetics</topic><topic>Pulmonary Surfactants - deficiency</topic><topic>Pulmonary Surfactants - genetics</topic><topic>Repetitive Sequences, Nucleic Acid - genetics</topic><topic>Respiratory Distress Syndrome, Newborn - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Deletion</topic><topic>Sequence Homology, Nucleic Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Floros, J</creatorcontrib><creatorcontrib>Veletza, S V</creatorcontrib><creatorcontrib>Kotikalapudi, P</creatorcontrib><creatorcontrib>Krizkova, L</creatorcontrib><creatorcontrib>Karinch, A M</creatorcontrib><creatorcontrib>Friedman, C</creatorcontrib><creatorcontrib>Buchter, S</creatorcontrib><creatorcontrib>Marks, K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Floros, J</au><au>Veletza, S V</au><au>Kotikalapudi, P</au><au>Krizkova, L</au><au>Karinch, A M</au><au>Friedman, C</au><au>Buchter, S</au><au>Marks, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome</atitle><jtitle>Biochemical journal</jtitle><addtitle>Biochem J</addtitle><date>1995-01-15</date><risdate>1995</risdate><volume>305 ( Pt 2)</volume><issue>2</issue><spage>583</spage><epage>590</epage><pages>583-590</pages><issn>0264-6021</issn><eissn>1470-8728</eissn><abstract>Pulmonary surfactant, a lipoprotein complex, is essential for normal lung function, and deficiency of surfactant can result in respiratory-distress syndrome (RDS) in the prematurely born infant. Some studies have pointed towards a genetic contribution to the aetiology of RDS. Because the surfactant protein B (SP-B) is important for optimal surfactant function and because it is involved in the pathogenesis of pulmonary disease, we investigated the genetic variability of the SP-B gene in individuals with and without RDS. We identified a 2.5 kb BamHI polymorphism and studied its location, nature and frequency. We localized this polymorphism in the first half of intron 4 and found that it is derived by gain or loss in the number of copies of a motif that consists of two elements, a 20 bp conserved sequence and a variable number of CA dinucleotides. Variability in the number of motifs resulting from either deletion (in 55.3% of the cases with the variation) or insertion (44.7%) of motifs was observed in genomic DNAs from unrelated individuals. Analysis of 219 genomic DNAs from infants with (n = 82) and without (n = 137) RDS showed that this insertion/deletion appears with significantly higher frequency in the RDS population (29.3 as against 16.8%, P &lt; 0.05).</abstract><cop>England</cop><pmid>7832777</pmid><doi>10.1042/bj3050583</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0264-6021
ispartof Biochemical journal, 1995-01, Vol.305 ( Pt 2) (2), p.583-590
issn 0264-6021
1470-8728
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1136402
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection
subjects African Continental Ancestry Group
Base Sequence
Cloning, Molecular
Deoxyribonuclease BamHI
European Continental Ancestry Group
Gene Frequency
Genetic Variation
Genome, Human
Humans
Infant
Infant, Newborn
Introns - genetics
Molecular Sequence Data
Mutagenesis, Insertional
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
Proteolipids - genetics
Pulmonary Surfactants - deficiency
Pulmonary Surfactants - genetics
Repetitive Sequences, Nucleic Acid - genetics
Respiratory Distress Syndrome, Newborn - genetics
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Nucleic Acid
title Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T13%3A24%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dinucleotide%20repeats%20in%20the%20human%20surfactant%20protein-B%20gene%20and%20respiratory-distress%20syndrome&rft.jtitle=Biochemical%20journal&rft.au=Floros,%20J&rft.date=1995-01-15&rft.volume=305%20(%20Pt%202)&rft.issue=2&rft.spage=583&rft.epage=590&rft.pages=583-590&rft.issn=0264-6021&rft.eissn=1470-8728&rft_id=info:doi/10.1042/bj3050583&rft_dat=%3Cpubmed_cross%3E7832777%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/7832777&rfr_iscdi=true