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      Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles

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          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.

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          Most cited references44

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          Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

          Fragile X syndrome is the most frequent form of inherited mental retardation and is associated with a fragile site at Xq27.3. We identified human YAC clones that span fragile X site-induced translocation breakpoints coincident with the fragile X site. A gene (FMR-1) was identified within a four cosmid contig of YAC DNA that expresses a 4.8 kb message in human brain. Within a 7.4 kb EcoRI genomic fragment, containing FMR-1 exonic sequences distal to a CpG island previously shown to be hypermethylated in fragile X patients, is a fragile X site-induced breakpoint cluster region that exhibits length variation in fragile X chromosomes. This fragment contains a lengthy CGG repeat that is 250 bp distal of the CpG island and maps within a FMR-1 exon. Localization of the brain-expressed FMR-1 gene to this EcoRI fragment suggests the involvement of this gene in the phenotypic expression of the fragile X syndrome.
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            The origins, patterns and implications of human spontaneous mutation.

            J F Crow (2000)
            The germline mutation rate in human males, especially older males, is generally much higher than in females, mainly because in males there are many more germ-cell divisions. However, there are some exceptions and many variations. Base substitutions, insertion-deletions, repeat expansions and chromosomal changes each follow different rules. Evidence from evolutionary sequence data indicates that the overall rate of deleterious mutation may be high enough to have a large effect on human well-being. But there are ways in which the impact of deleterious mutations can be mitigated.
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              Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

              Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT. Age at onset has been used as a quantitative phenotype in genetic analysis looking for Huntington's disease modifiers, but is hard to define and not always available. Therefore, we aimed to generate a novel measure of disease progression and to identify genetic markers associated with this progression measure.
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                Author and article information

                Contributors
                sallynolin@gmail.com
                Journal
                Am J Med Genet A
                Am. J. Med. Genet. A
                10.1002/(ISSN)1552-4833
                AJMG
                American Journal of Medical Genetics. Part a
                John Wiley & Sons, Inc. (Hoboken, USA )
                1552-4825
                1552-4833
                02 May 2019
                July 2019
                : 179
                : 7 ( doiID: 10.1002/ajmg.a.v179.7 )
                : 1148-1156
                Affiliations
                [ 1 ] Department of Human Genetics New York State Institute for Basic Research in Developmental Disabilities Staten Island New York
                [ 2 ] Department of Human Genetics Emory University School of Medicine Atlanta Georgia
                [ 3 ] Wessex Regional Genetics Laboratory Salisbury NHS District Hospital Salisbury United Kingdom
                [ 4 ] Biochemical and Molecular Genetics Hospital Clinic de Barcelona, IDIBAPS and CIBERER Barcelona Spain
                [ 5 ] Department of Genetics and Evolutionary Biology, Institute of Biosciences Universidade de São Paulo São Paulo Brazil
                [ 6 ] Asuragen, Inc. Austin Texas
                Author notes
                [*] [* ] Correspondence

                Sarah L. Nolin, Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314.

                Email: sallynolin@ 123456gmail.com

                Author information
                https://orcid.org/0000-0001-5209-289X
                https://orcid.org/0000-0002-7906-0916
                Article
                AJMGA61165
                10.1002/ajmg.a.61165
                6619443
                31050164
                4e0a7612-41d6-42a7-b9bc-4fe8777aa5c8
                © 2019 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 January 2019
                : 21 March 2019
                : 11 April 2019
                Page count
                Figures: 2, Tables: 7, Pages: 9, Words: 7964
                Funding
                Funded by: New York State Institute for Basic Research in Developmental Disabilities
                Funded by: New York State Office for People with Developmental Disabilities
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                ajmga61165
                July 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.5 mode:remove_FC converted:10.07.2019

                Genetics
                fmr1,fragile x,trinucleotide repeat instability
                Genetics
                fmr1, fragile x, trinucleotide repeat instability

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