Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene

被引:2
|
作者
Quilichini, Juliette [1 ]
Perol, Sandrine [2 ]
Cuisset, Laurence [1 ]
Grotto, Sarah [3 ]
Fouveaut, Corinne [1 ]
Barbot, Jean Claude [1 ]
Verebi, Camille [1 ]
Jordan, Penelope [1 ]
Heron, Delphine [4 ]
Molina-Gomes, Denise [5 ]
Pipiras, Eva [6 ]
Grynberg, Michael [7 ]
Catteau-Jonard, Sophie [8 ]
Touraine, Philippe [9 ]
Christin-Maitre, Sophie [10 ]
Plu-Bureau, Genevieve [2 ]
El Khattabi, Laila [1 ,11 ,13 ,14 ]
Bienvenu, Thierry [1 ,12 ]
机构
[1] Ctr Univ Paris Cite, APHP, Serv Medecine Genom Malad Syst & organe, Paris, France
[2] Ctr Univ Paris Cite, Hop Cochin Port Royal, APHP, Unite gynecol med, Paris, France
[3] Ctr Univ Paris Cite, Hop Cochin, APHP, Matern Port Royal, Paris, France
[4] Sorbonne Univ, Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France
[5] CHI Poissy St Germain, Serv Biol Reprod Cytogenet & Genet Med, Poissy, France
[6] Univ Sorbonne Paris Nord, Hop Jean Verdier, Unite fonct Medecine genom & genet Clin, APHP, Bondy, France
[7] Hop Jean Verdier, Gynecol med & medecine Reprod, Bondy, France
[8] Univ Lille, Serv Gynecol Medicale, CHU Lille, Lille, France
[9] Sorbonne Univ, Pitie Salpetriere Hosp, APHP, Dept Endocrinol & medecine Reprod,Ctr Rare Endocri, Paris, France
[10] Sorbonne Univ, Serv endocrinol diabetol & medecine Reprod, APHP, Paris, France
[11] Inst Cochin, Team gametes birth, INSERM U1016, Paris, France
[12] Hop Cochin, Serv Medecine Genom Malad Syst & organe, F-75014 Paris, France
[13] Hop La Pitie Salpetriere, Dept Genet medicale, F-75013 Paris, France
[14] Sorbonne Univ, Hop Armand Trousseau, Dept Genet medicale, Unite fonct Genom Chromos, Paris, France
关键词
diminished ovarian reserve; FMR1; FMR1 allelic complexity score; gray zone expansion; premature ovarian insufficiency; premutation; FRAGILE-X PREMUTATION; CGG REPEATS; NORMAL RANGE; ASSOCIATION; FAILURE; WOMEN; MENOPAUSE; RESERVE; NUMBER; AGE;
D O I
10.1002/ajmg.a.63479
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
FMR1 premutation female carriers are at risk of developing premature/primary ovarian insufficiency (POI) with an incomplete penetrance. In this study, we determined the CGG repeat size among 1095 women with diminished ovarian reserve (DOR) / POI and characterized the CGG/AGG substructure in 44 women carrying an abnormal FMR1 repeat expansion number, compared to a group of 25 pregnant women carrying an abnormal FMR1 CGG repeat size. Allelic complexity scores of the FMR1 gene were calculated and compared between the two groups. In the DOR/POI cohort, 2.1% of women presented with an intermediate repeat size and 1.9% with a premutation. Our results suggest that the risk of POI is highest in the mid-range of CGG repeats. We observed that the allelic score is significantly higher in POI women compared to the pregnant women group (p-value = 0.02). We suggest that a high allelic score due to more than 2 AGG interspersions in the context of an intermediate number of repetitions could favor POI. Larger studies are still needed to evaluate the relevance of this new tool for the determination of the individual risk of developing POI in women with abnormal number of CGG repeats.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes
    Madrigal, Irene
    Xuncla, Mar
    Isabel Tejada, Maria
    Martinez, Francisco
    Fernandez-Carvajal, Isabel
    Alberto Perez-Jurado, Luis
    Rodriguez-Revenga, Laia
    Mila, Montserrat
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (08) : 921 - 923
  • [22] A family with two female siblings with compound heterozygous FMR1 premutation alleles
    Basuta, K.
    Lozano, R.
    Schneider, A.
    Yrigollen, C. M.
    Hessl, D.
    Hagerman, R. J.
    Tassone, F.
    CLINICAL GENETICS, 2014, 85 (05) : 458 - 463
  • [23] CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles
    Pretto, Dalyir I.
    Mendoza-Morales, Guadalupe
    Lo, Joyce
    Cao, Ru
    Hadd, Andrew
    Latham, Gary J.
    Durbin-Johnson, Blythe
    Hagerman, Randi
    Tassone, Flora
    JOURNAL OF MEDICAL GENETICS, 2014, 51 (05) : 309 - 318
  • [24] Prevalence of Cytogenetic Abnormalities and FMR1 Gene Premutation in a Portuguese Population with Premature Ovarian Insufficiency
    Neves, Ana Raquel
    Pais, Ana Sofia
    Ferreira, Susana Isabel
    Ramos, Vera
    Carvalho, Maria Joao
    Estevinho, Alexandra
    Matoso, Eunice
    Geraldes, Fernanda
    Carreira, Isabel Marques
    Aguas, Fernanda
    ACTA MEDICA PORTUGUESA, 2021, 34 (09): : 580 - 585
  • [25] Evaluation of FMR1 gene premutation in Sardinians with multiple sclerosis
    Cocco, E.
    Tranquilli, S.
    Murru, M. R.
    Frau, J.
    Lorefice, L.
    Mamusa, E.
    Fenu, G.
    Coghe, G.
    Marrosu, M. G.
    MULTIPLE SCLEROSIS JOURNAL, 2011, 17 : S333 - S333
  • [26] FMR1 mRNA derived from premutation alleles is translated with reduced efficiency
    Bagni, C
    Tassone, F
    Primerano, B
    Ludwig, A
    Mamay, C
    Hagerman, R
    Hagerman, P
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 338 - 338
  • [27] Familial occurrence of FXTAS caused by premutation in the FMR1 gene
    Koziorowski, Dariusz
    Rajkiewicz, Marta
    Sulek-Piatkowska, Anna
    Zarembo, Jacek
    Kaca-Orynska, Malgorzata
    Mandat, Tomasz
    Friedman, Andrzej
    NEUROLOGIA I NEUROCHIRURGIA POLSKA, 2011, 45 (04) : 391 - 396
  • [28] Elevated Levels of FMR1 mRNA in Granulosa Cells Are Associated with Low Ovarian Reserve in FMR1 Premutation Carriers
    Elizur, Shai E.
    Lebovitz, Oshrit
    Derech-Haim, Sanaz
    Dratviman-Storobinsky, Olga
    Feldman, Baruch
    Dor, Jehoshua
    Orvieto, Raoul
    Cohen, Yoram
    PLOS ONE, 2014, 9 (08):
  • [29] The FMR1 premutation carrier and the premature ovarian failure phenotype.
    Sullivan, AK
    Shubeck, LJ
    Allen, EG
    He, W
    Paquin, JJ
    Leslie, ML
    Scott, LH
    Sherman, SL
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 506 - 506
  • [30] The FMR1 premutation as a cause of premature ovarian failure in Brazilian women
    Costa, Silvia S.
    da Fonseca, Angela M.
    Bagnoli, Vicente R.
    Vianna-Morgantel, Angela M.
    GENETICS AND MOLECULAR BIOLOGY, 2006, 29 (03) : 423 - 428