International Journal of Women's Health Dovepress the Genetics of Premature Ovarian Failure: Current Perspectives

Premature ovarian failure (POF) is a common cause of infertility in women, characterized by amenorrhea, hypoestrogenism, and elevated gonadotropin levels in women under the age of 40. Many genes have been identified over the past few years that contribute to the development of POF. However, few genes have been identified that can explain a substantial proportion of cases of POF. The unbiased approaches of genome-wide association studies and next-generation sequencing technologies have identified several novel genes implicated in POF. As only a small proportion of genes influencing idiopathic POF have been identified thus far, it remains to be determined how many genes and molecular pathways may influence idiopathic POF development. However, owing to POF's diverse etiology and genetic hetero-geneity, we expect to see the contribution of several new and novel molecular pathways that will greatly enhance our understanding of the regulation of ovarian function. Future genetic studies in large cohorts of well-defined, unrelated, idiopathic POF patients will provide a great opportunity to identify the missing heritability of idiopathic POF. The identification of several causative genes may allow for early detection and would provide better opportunity for early intervention, and furthermore, the identification of specific gene defects will help direct potential targets for future treatment.

[1]  P. Laissue,et al.  Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations. , 2015, Fertility and sterility.

[2]  Shidou Zhao,et al.  MicroRNA-22-3p is down-regulated in the plasma of Han Chinese patients with premature ovarian failure. , 2015, Fertility and sterility.

[3]  R. Dalgleish,et al.  Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency. , 2015, Fertility and sterility.

[4]  U. Surti,et al.  Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability. , 2015, Journal of Clinical Investigation.

[5]  F. Adami,et al.  ESR1 and ESR2 gene polymorphisms are associated with human reproduction outcomes in Brazilian women , 2014, Journal of Ovarian Research.

[6]  U. Surti,et al.  MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability. , 2014, American journal of human genetics.

[7]  Jie Wu,et al.  Gene variation and premature ovarian failure: a meta-analysis. , 2014, European journal of obstetrics, gynecology, and reproductive biology.

[8]  Y. T. van der Schouw,et al.  The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency. , 2014, Human reproduction.

[9]  Leslie G Biesecker,et al.  Diagnostic clinical genome and exome sequencing. , 2014, The New England journal of medicine.

[10]  R. Dalgleish,et al.  Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure. , 2014, Fertility and sterility.

[11]  R. Veitia,et al.  Mutant cohesin in premature ovarian failure. , 2014, The New England journal of medicine.

[12]  Bai-Lin Wu,et al.  Mutations in HFM1 in recessive primary ovarian insufficiency. , 2014, The New England journal of medicine.

[13]  N. Kim,et al.  Association of inhibin α gene promoter polymorphisms with risk of idiopathic primary ovarian insufficiency in Korean women. , 2014, Maturitas.

[14]  J. Murabito,et al.  Genome-wide association studies of age at menarche and age at natural menopause , 2014, Molecular and Cellular Endocrinology.

[15]  A. Rajkovic,et al.  Genomic Markers of Ovarian Reserve , 2013, Seminars in Reproductive Medicine.

[16]  P. Scaruffi,et al.  Insight into the Genomics of Premature Ovarian Failure , 2013 .

[17]  Kathryn J. Woad,et al.  FSH receptor gene variants are rarely associated with premature ovarian failure. , 2013, Reproductive biomedicine online.

[18]  E. Demerath,et al.  A genome-wide association study of early menopause and the combined impact of identified variants , 2013, Human molecular genetics.

[19]  C. Peluso,et al.  Risk of premature ovarian failure is associated to the PvuII polymorphism at estrogen receptor gene ESR1 , 2012, Journal of Assisted Reproduction and Genetics.

[20]  Ying Zhou,et al.  Differentially expressed plasma microRNAs in premature ovarian failure patients and the potential regulatory function of mir-23a in granulosa cell apoptosis. , 2012, Reproduction.

[21]  C. Carlson,et al.  Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study. , 2012, Human molecular genetics.

[22]  W. Newman,et al.  Follicle-stimulating hormone receptor gene polymorphisms are not associated with ovarian reserve markers. , 2012, Fertility and sterility.

[23]  C. Wijmenga,et al.  Copy number variants on the X chromosome in women with primary ovarian insufficiency. , 2011, Fertility and sterility.

[24]  A. Rajkovic,et al.  Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure. , 2011, Fertility and sterility.

[25]  D. Christofolini,et al.  Genetic aspects of premature ovarian failure: a literature review , 2011, Archives of Gynecology and Obstetrics.

[26]  L. B. Rangel,et al.  Evaluation of PvuII and XbaI polymorphisms in the estrogen receptor alpha gene (ESR1) in relation to menstrual cycle timing and reproductive parameters in post-menopausal women. , 2010, Maturitas.

[27]  L. Persani,et al.  Genes involved in human premature ovarian failure. , 2010, Journal of molecular endocrinology.

[28]  A. Shelling Premature ovarian failure. , 2010, Reproduction.

[29]  A. Ashworth,et al.  Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study , 2010, Human molecular genetics.

[30]  A. Röpke,et al.  Copy Number Variants in Premature Ovarian Failure and Ovarian Dysgenesis , 2010, Sexual Development.

[31]  L. Singh,et al.  Genes governing premature ovarian failure. , 2010, Reproductive biomedicine online.

[32]  S. Costagliola,et al.  Variants of the BMP15 gene in a cohort of patients with premature ovarian failure. , 2010, Human reproduction.

[33]  G. Tachdjian,et al.  Genome-wide association study and premature ovarian failure. , 2010, Annales d'endocrinologie.

[34]  K. McElreavey,et al.  NR5A1/SF-1 and development and function of the ovary. , 2010, Annales d'endocrinologie.

[35]  Sue-Kyung Park,et al.  Estrogen receptor-1 genetic polymorphisms for the risk of premature ovarian failure and early menopause. , 2010, Journal of women's health.

[36]  Binbin Wang,et al.  Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure , 2010, Clinical endocrinology.

[37]  R. Frydman,et al.  Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure. , 2009, The Journal of clinical endocrinology and metabolism.

[38]  A. Shelling Progress in the study of genetic disease: bringing new light to complex problems , 2009, Postgraduate Medical Journal.

[39]  S. Bione,et al.  A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. , 2009, Human reproduction.

[40]  P. Touraine,et al.  Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failure. , 2009, European journal of endocrinology.

[41]  A. Hofman,et al.  Loci at chromosomes 13, 19 and 20 influence age at natural menopause , 2009, Nature Genetics.

[42]  S. Bione,et al.  BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein , 2009, Human mutation.

[43]  Zi-jiang Chen,et al.  Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure. , 2009, Fertility and sterility.

[44]  K. McElreavey,et al.  Mutations in NR5A1 associated with ovarian insufficiency. , 2009, The New England journal of medicine.

[45]  C. Wijmenga,et al.  Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. , 2009, Human reproduction.

[46]  A. Rajkovic,et al.  Germ Cell-Specific Transcriptional Regulator Sohlh2 Is Essential for Early Mouse Folliculogenesis and Oocyte-Specific Gene Expression1 , 2008, Biology of reproduction.

[47]  B. Bianco,et al.  Clinical implications of the detection of Y-chromosome mosaicism in Turner's syndrome: report of 3 cases. , 2008, Fertility and sterility.

[48]  A. Rajkovic,et al.  Transcription factor FIGLA is mutated in patients with premature ovarian failure. , 2008, American journal of human genetics.

[49]  N. Kim,et al.  Parathyroid hormone-responsive B1 gene is associated with premature ovarian failure. , 2008, Human reproduction.

[50]  A. Rajkovic,et al.  Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure. , 2007, Fertility and sterility.

[51]  A. Shelling,et al.  Genetic variation in human disease and a new role for copy number variants. , 2007, Mutation research.

[52]  A. Rajkovic,et al.  NOBOX homeobox mutation causes premature ovarian failure. , 2007, American journal of human genetics.

[53]  M. Epstein,et al.  Examination of reproductive aging milestones among women who carry the FMR1 premutation. , 2007, Human reproduction.

[54]  C. Martínez-Labarga,et al.  Estrogen receptor alpha polymorphisms and fertility in populations with different reproductive patterns. , 2007, Molecular human reproduction.

[55]  Michael Q. Zhang,et al.  Critical roles for Dicer in the female germline. , 2007, Genes & development.

[56]  R. Frydman,et al.  Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. , 2006, European journal of endocrinology.

[57]  L. Nelson,et al.  Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure. , 2006, The Journal of clinical endocrinology and metabolism.

[58]  L. Singh,et al.  Missense mutations in the BMP15 gene are associated with ovarian failure , 2006, Human Genetics.

[59]  L. Singh,et al.  Mutational screening of the coding region of growth differentiation factor 9 gene in Indian women with ovarian failure , 2005, Menopause.

[60]  N. Suzumori,et al.  Mutational analysis of the homeobox region of the human NOBOX gene in Japanese women who exhibit premature ovarian failure. , 2005, Fertility and sterility.

[61]  S. Shimasaki,et al.  Posttranslational processing of mouse and human BMP-15: potential implication in the determination of ovulation quota. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[62]  Martin M Matzuk,et al.  NOBOX Deficiency Disrupts Early Folliculogenesis and Oocyte-Specific Gene Expression , 2004, Science.

[63]  L. Singh,et al.  Mutational analysis of the mature peptide region of inhibin genes in Indian women with ovarian failure. , 2004, Human reproduction.

[64]  R. Behringer,et al.  Cell-specific knockout of steroidogenic factor 1 reveals its essential roles in gonadal function. , 2004, Molecular endocrinology.

[65]  Katrin Anlag,et al.  The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance , 2004, Development.

[66]  A. Shelling,et al.  Identification of novel mutations in FOXL2 associated with premature ovarian failure. , 2002, Molecular human reproduction.

[67]  C. Porta,et al.  Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure. , 2002, Human reproduction.

[68]  M. Ascoli,et al.  The lutropin/choriogonadotropin receptor, a 2002 perspective. , 2002, Endocrine reviews.

[69]  D. Schlessinger,et al.  The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome , 2001, Nature Genetics.

[70]  A. Caudy,et al.  Role for a bidentate ribonuclease in the initiation step of RNA interference , 2001 .

[71]  A. Shelling,et al.  Inhibin: a candidate gene for premature ovarian failure. , 2000, Human reproduction.

[72]  K. Takakura,et al.  Mutation analysis of the growth differentiation factor-9 and -9B genes in patients with premature ovarian failure and polycystic ovary syndrome. , 2000, Fertility and sterility.

[73]  I. Huhtaniemi,et al.  The effect of a null mutation in the follicle-stimulating hormone receptor gene on mouse reproduction. , 2000, Endocrinology.

[74]  J. Findlay,et al.  The role of estrogen in folliculogenesis , 1999, Molecular and Cellular Endocrinology.

[75]  W. Brown,et al.  Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data. , 1999, American journal of medical genetics.

[76]  M. Matzuk,et al.  The bone morphogenetic protein 15 gene is X-linked and expressed in oocytes. , 1998, Molecular endocrinology.

[77]  A. Latronico,et al.  A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor. , 1998, Molecular endocrinology.

[78]  L. Layman,et al.  The Finnish follicle-stimulating hormone receptor gene mutation is rare in North American women with 46,XX ovarian failure. , 1998, Fertility and sterility.

[79]  L. Liang,et al.  FIGalpha, a germ cell specific transcription factor involved in the coordinate expression of the zona pellucida genes. , 1997, Development.

[80]  David F. Albertini,et al.  Growth differentiation factor-9 is required during early ovarian folliculogenesis , 1996, Nature.

[81]  A. Chapelle,et al.  Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure , 1995, Cell.

[82]  R. Laxová,et al.  The critical region on the human Xq , 1990, Human Genetics.

[83]  R. Rebar,et al.  Triple-X Syndrome and Premature Ovarian Failure , 1983, Obstetrics and gynecology.

[84]  R. Dorfman,et al.  High genetic heterogeneity of Premature Ovarian Insufficiency From DNA replication and repair to hormonal regulation , 2014 .

[85]  Uimc Helq Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways , 2012 .

[86]  L. Persani,et al.  Genetic defects of ovarian TGF-β-like factors and premature ovarian failure. , 2011, Journal of endocrinological investigation.

[87]  A. Shelling,et al.  Inhibin and premature ovarian failure. , 2010, Human reproduction update.

[88]  P. Chambon,et al.  Theca-Specific Estrogen Receptor-Knockout Mice Lose Fertility Prematurely , 2009 .

[89]  A. Meikle Estrogen receptor α gene polymorphisms are associated with idiopathic premature ovarian failure , 2008 .

[90]  J. Dias,et al.  Molecular, structural, and cellular biology of follitropin and follitropin receptor. , 2002, Vitamins and hormones.

[91]  G. Conway,et al.  Genetic basis of premature ovarian failure. , 1998, Human fertility.

[92]  M. Gassmann,et al.  Tissue-specific expression of a FMR1/beta-galactosidase fusion gene in transgenic mice. , 1995, Human molecular genetics.

[93]  Adriana Coutinho de Azevedo Guimarães,et al.  International Journal of Women's Health , 2022 .