Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles
Instability of the FMR1 repeat, commonly observed in transmissions of premutation alleles (55–200 repeats), is influenced by the size of the repeat, its internal structure and the sex of the transmitting parent. We assessed these three factors in unstable transmissions of 14/3,335 normal (~5 to 44 r...
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Veröffentlicht in: | American journal of medical genetics. Part A 2019-07, Vol.179 (7), p.1148-1156 |
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creator | Nolin, Sarah L. Glicksman, Anne Tortora, Nicole Allen, Emily Macpherson, James Mila, Montserrat Vianna‐Morgante, Angela M. Sherman, Stephanie L. Dobkin, Carl Latham, Gary J. Hadd, Andrew G. |
description | Instability of the FMR1 repeat, commonly observed in transmissions of premutation alleles (55–200 repeats), is influenced by the size of the repeat, its internal structure and the sex of the transmitting parent. We assessed these three factors in unstable transmissions of 14/3,335 normal (~5 to 44 repeats), 54/293 intermediate (45–54 repeats), and 1561/1,880 premutation alleles. While most unstable transmissions led to expansions, contractions to smaller repeats were observed in all size classes. For normal alleles, instability was more frequent in paternal transmissions and in alleles with long 3′ uninterrupted repeat lengths. For premutation alleles, contractions also occurred more often in paternal than maternal transmissions and the frequency of paternal contractions increased linearly with repeat size. All paternal premutation allele contractions were transmitted as premutation alleles, but maternal premutation allele contractions were transmitted as premutation, intermediate, or normal alleles. The eight losses of AGG interruptions in the FMR1 repeat occurred exclusively in contractions of maternal premutation alleles. We propose a refined model of FMR1 repeat progression from normal to premutation size and suggest that most normal alleles without AGG interruptions are derived from contractions of maternal premutation alleles. |
doi_str_mv | 10.1002/ajmg.a.61165 |
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We assessed these three factors in unstable transmissions of 14/3,335 normal (~5 to 44 repeats), 54/293 intermediate (45–54 repeats), and 1561/1,880 premutation alleles. While most unstable transmissions led to expansions, contractions to smaller repeats were observed in all size classes. For normal alleles, instability was more frequent in paternal transmissions and in alleles with long 3′ uninterrupted repeat lengths. For premutation alleles, contractions also occurred more often in paternal than maternal transmissions and the frequency of paternal contractions increased linearly with repeat size. All paternal premutation allele contractions were transmitted as premutation alleles, but maternal premutation allele contractions were transmitted as premutation, intermediate, or normal alleles. The eight losses of AGG interruptions in the FMR1 repeat occurred exclusively in contractions of maternal premutation alleles. We propose a refined model of FMR1 repeat progression from normal to premutation size and suggest that most normal alleles without AGG interruptions are derived from contractions of maternal premutation alleles.</description><identifier>ISSN: 1552-4825</identifier><identifier>ISSN: 1552-4833</identifier><identifier>EISSN: 1552-4833</identifier><identifier>DOI: 10.1002/ajmg.a.61165</identifier><identifier>PMID: 31050164</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Alleles ; Female ; FMR1 ; FMR1 protein ; fragile X ; Fragile X Mental Retardation Protein - genetics ; Fragile X Syndrome - diagnosis ; Fragile X Syndrome - genetics ; Fragile X Syndrome - pathology ; Gene Expression ; Gene Frequency ; Humans ; Inheritance Patterns ; Male ; Original ; Pedigree ; Trinucleotide Repeat Expansion ; trinucleotide repeat instability</subject><ispartof>American journal of medical genetics. 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Part A</title><addtitle>Am J Med Genet A</addtitle><description>Instability of the FMR1 repeat, commonly observed in transmissions of premutation alleles (55–200 repeats), is influenced by the size of the repeat, its internal structure and the sex of the transmitting parent. We assessed these three factors in unstable transmissions of 14/3,335 normal (~5 to 44 repeats), 54/293 intermediate (45–54 repeats), and 1561/1,880 premutation alleles. While most unstable transmissions led to expansions, contractions to smaller repeats were observed in all size classes. For normal alleles, instability was more frequent in paternal transmissions and in alleles with long 3′ uninterrupted repeat lengths. For premutation alleles, contractions also occurred more often in paternal than maternal transmissions and the frequency of paternal contractions increased linearly with repeat size. All paternal premutation allele contractions were transmitted as premutation alleles, but maternal premutation allele contractions were transmitted as premutation, intermediate, or normal alleles. The eight losses of AGG interruptions in the FMR1 repeat occurred exclusively in contractions of maternal premutation alleles. We propose a refined model of FMR1 repeat progression from normal to premutation size and suggest that most normal alleles without AGG interruptions are derived from contractions of maternal premutation alleles.</description><subject>Alleles</subject><subject>Female</subject><subject>FMR1</subject><subject>FMR1 protein</subject><subject>fragile X</subject><subject>Fragile X Mental Retardation Protein - genetics</subject><subject>Fragile X Syndrome - diagnosis</subject><subject>Fragile X Syndrome - genetics</subject><subject>Fragile X Syndrome - pathology</subject><subject>Gene Expression</subject><subject>Gene Frequency</subject><subject>Humans</subject><subject>Inheritance Patterns</subject><subject>Male</subject><subject>Original</subject><subject>Pedigree</subject><subject>Trinucleotide Repeat Expansion</subject><subject>trinucleotide repeat instability</subject><issn>1552-4825</issn><issn>1552-4833</issn><issn>1552-4833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp9kUtvEzEURi0Eog_YsUaW2LBIUj_Hkw1SFLUB1AoJwdq6mbnTTuSxB3uGPn49TtJGwKIrW_bR0f3uR8g7zmacMXEGm-56BrOC80K_IMdcazFVpZQvD3ehj8hJShvGJNOmeE2OJGea8UIdk4fzux58aoNPFHxNq-CHCNWwewgNHW6QXlx953S5WtGIPcJAW0_1RLOSZtKnrk3pifYhduAmmRgwdli3MOBk5-0jduMAWy8F59BhekNeNeASvn08T8nPi_Mfy8_Ty2-rL8vF5bRS2uhpbUzNhBIFlKrha9nwkjVSGclNDWJdzw3kKM1c5mVABUaXhq8VqAZBopa1PCWf9t5-XOeZKtwmdLaPbQfx3gZo7b8_vr2x1-G3LQo-V0pmwcdHQQy_RkyDzZkrdA48hjFZIcRcSJM3mtEP_6GbMEaf42VKmjy1MkWmJnuqiiGliM1hGM7stlS7LdWC3ZWa8fd_BzjATy1mQO2B29bh_bMyu_h6tVrsvX8A27WuSQ</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Nolin, Sarah L.</creator><creator>Glicksman, Anne</creator><creator>Tortora, Nicole</creator><creator>Allen, Emily</creator><creator>Macpherson, James</creator><creator>Mila, Montserrat</creator><creator>Vianna‐Morgante, Angela M.</creator><creator>Sherman, Stephanie L.</creator><creator>Dobkin, Carl</creator><creator>Latham, Gary J.</creator><creator>Hadd, Andrew G.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</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>7QP</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7906-0916</orcidid><orcidid>https://orcid.org/0000-0001-5209-289X</orcidid></search><sort><creationdate>201907</creationdate><title>Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles</title><author>Nolin, Sarah L. ; Glicksman, Anne ; Tortora, Nicole ; Allen, Emily ; Macpherson, James ; Mila, Montserrat ; Vianna‐Morgante, Angela M. ; Sherman, Stephanie L. ; Dobkin, Carl ; Latham, Gary J. ; Hadd, Andrew G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4575-d77d02426a84f1b3f180f347317da2bd97a016f93002aca75871b4a4fea3e53d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alleles</topic><topic>Female</topic><topic>FMR1</topic><topic>FMR1 protein</topic><topic>fragile X</topic><topic>Fragile X Mental Retardation Protein - genetics</topic><topic>Fragile X Syndrome - diagnosis</topic><topic>Fragile X Syndrome - genetics</topic><topic>Fragile X Syndrome - pathology</topic><topic>Gene Expression</topic><topic>Gene Frequency</topic><topic>Humans</topic><topic>Inheritance Patterns</topic><topic>Male</topic><topic>Original</topic><topic>Pedigree</topic><topic>Trinucleotide Repeat Expansion</topic><topic>trinucleotide repeat instability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nolin, Sarah L.</creatorcontrib><creatorcontrib>Glicksman, Anne</creatorcontrib><creatorcontrib>Tortora, Nicole</creatorcontrib><creatorcontrib>Allen, Emily</creatorcontrib><creatorcontrib>Macpherson, James</creatorcontrib><creatorcontrib>Mila, Montserrat</creatorcontrib><creatorcontrib>Vianna‐Morgante, Angela M.</creatorcontrib><creatorcontrib>Sherman, Stephanie L.</creatorcontrib><creatorcontrib>Dobkin, Carl</creatorcontrib><creatorcontrib>Latham, Gary J.</creatorcontrib><creatorcontrib>Hadd, Andrew G.</creatorcontrib><collection>Wiley Online Library 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>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of medical genetics. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nolin, Sarah L.</au><au>Glicksman, Anne</au><au>Tortora, Nicole</au><au>Allen, Emily</au><au>Macpherson, James</au><au>Mila, Montserrat</au><au>Vianna‐Morgante, Angela M.</au><au>Sherman, Stephanie L.</au><au>Dobkin, Carl</au><au>Latham, Gary J.</au><au>Hadd, Andrew G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles</atitle><jtitle>American journal of medical genetics. Part A</jtitle><addtitle>Am J Med Genet A</addtitle><date>2019-07</date><risdate>2019</risdate><volume>179</volume><issue>7</issue><spage>1148</spage><epage>1156</epage><pages>1148-1156</pages><issn>1552-4825</issn><issn>1552-4833</issn><eissn>1552-4833</eissn><abstract>Instability of the FMR1 repeat, commonly observed in transmissions of premutation alleles (55–200 repeats), is influenced by the size of the repeat, its internal structure and the sex of the transmitting parent. We assessed these three factors in unstable transmissions of 14/3,335 normal (~5 to 44 repeats), 54/293 intermediate (45–54 repeats), and 1561/1,880 premutation alleles. While most unstable transmissions led to expansions, contractions to smaller repeats were observed in all size classes. For normal alleles, instability was more frequent in paternal transmissions and in alleles with long 3′ uninterrupted repeat lengths. For premutation alleles, contractions also occurred more often in paternal than maternal transmissions and the frequency of paternal contractions increased linearly with repeat size. All paternal premutation allele contractions were transmitted as premutation alleles, but maternal premutation allele contractions were transmitted as premutation, intermediate, or normal alleles. The eight losses of AGG interruptions in the FMR1 repeat occurred exclusively in contractions of maternal premutation alleles. We propose a refined model of FMR1 repeat progression from normal to premutation size and suggest that most normal alleles without AGG interruptions are derived from contractions of maternal premutation alleles.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>31050164</pmid><doi>10.1002/ajmg.a.61165</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7906-0916</orcidid><orcidid>https://orcid.org/0000-0001-5209-289X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Female FMR1 FMR1 protein fragile X Fragile X Mental Retardation Protein - genetics Fragile X Syndrome - diagnosis Fragile X Syndrome - genetics Fragile X Syndrome - pathology Gene Expression Gene Frequency Humans Inheritance Patterns Male Original Pedigree Trinucleotide Repeat Expansion trinucleotide repeat instability |
title | Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles |
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