#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Genome-Wide Association Studies Identify Two Novel Mutations Responsible for an Atypical Hyperprolificacy Phenotype in Sheep


Some sheep breeds are naturally prolific, and they are very informative for the studies of reproductive genetics and physiology. Major genes increasing litter size (LS) and ovulation rate (OR) were suspected in the French Grivette and the Polish Olkuska sheep populations, respectively. To identify genetic variants responsible for the highly prolific phenotype in these two breeds, genome-wide association studies (GWAS) followed by complementary genetic and functional analyses were performed. Highly prolific ewes (cases) and normal prolific ewes (controls) from each breed were genotyped using the Illumina OvineSNP50 Genotyping Beadchip. In both populations, an X chromosome region, close to the BMP15 gene, harbored clusters of markers with suggestive evidence of association at significance levels between 1E−05 and 1E−07. The BMP15 candidate gene was then sequenced, and two novel non-conservative mutations called FecXGr and FecXO were identified in the Grivette and Olkuska breeds, respectively. The two mutations were associated with the highly prolific phenotype (pFecXGr = 5.98E−06 and pFecXO = 2.55E−08). Homozygous ewes for the mutated allele showed a significantly increased prolificacy (FecXGr/FecXGr, LS = 2.50±0.65 versus FecX+/FecXGr, LS = 1.93±0.42, p<1E−03 and FecXO/FecXO, OR = 3.28±0.85 versus FecX+/FecXO, OR = 2.02±0.47, p<1E−03). Both mutations are located in very well conserved motifs of the protein and altered the BMP15 signaling activity in vitro using a BMP-responsive luciferase test in COV434 granulosa cells. Thus, we have identified two novel mutations in the BMP15 gene associated with increased LS and OR. Notably, homozygous FecXGr/FecXGr Grivette and homozygous FecXO/FecXO Olkuska ewes are hyperprolific in striking contrast with the sterility exhibited by all other known homozygous BMP15 mutations. Our results bring new insights into the key role played by the BMP15 protein in ovarian function and could contribute to a better understanding of the pathogenesis of women′s fertility disorders.


Vyšlo v časopise: Genome-Wide Association Studies Identify Two Novel Mutations Responsible for an Atypical Hyperprolificacy Phenotype in Sheep. PLoS Genet 9(4): e32767. doi:10.1371/journal.pgen.1003482
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003482

Souhrn

Some sheep breeds are naturally prolific, and they are very informative for the studies of reproductive genetics and physiology. Major genes increasing litter size (LS) and ovulation rate (OR) were suspected in the French Grivette and the Polish Olkuska sheep populations, respectively. To identify genetic variants responsible for the highly prolific phenotype in these two breeds, genome-wide association studies (GWAS) followed by complementary genetic and functional analyses were performed. Highly prolific ewes (cases) and normal prolific ewes (controls) from each breed were genotyped using the Illumina OvineSNP50 Genotyping Beadchip. In both populations, an X chromosome region, close to the BMP15 gene, harbored clusters of markers with suggestive evidence of association at significance levels between 1E−05 and 1E−07. The BMP15 candidate gene was then sequenced, and two novel non-conservative mutations called FecXGr and FecXO were identified in the Grivette and Olkuska breeds, respectively. The two mutations were associated with the highly prolific phenotype (pFecXGr = 5.98E−06 and pFecXO = 2.55E−08). Homozygous ewes for the mutated allele showed a significantly increased prolificacy (FecXGr/FecXGr, LS = 2.50±0.65 versus FecX+/FecXGr, LS = 1.93±0.42, p<1E−03 and FecXO/FecXO, OR = 3.28±0.85 versus FecX+/FecXO, OR = 2.02±0.47, p<1E−03). Both mutations are located in very well conserved motifs of the protein and altered the BMP15 signaling activity in vitro using a BMP-responsive luciferase test in COV434 granulosa cells. Thus, we have identified two novel mutations in the BMP15 gene associated with increased LS and OR. Notably, homozygous FecXGr/FecXGr Grivette and homozygous FecXO/FecXO Olkuska ewes are hyperprolific in striking contrast with the sterility exhibited by all other known homozygous BMP15 mutations. Our results bring new insights into the key role played by the BMP15 protein in ovarian function and could contribute to a better understanding of the pathogenesis of women′s fertility disorders.


Zdroje

1. MatzukMM, BurnsKH, ViveirosMM, EppigJJ (2002) Intercellular communication in the mammalian ovary: oocytes carry the conversation. Science 296: 2178–2180.

2. GilchristRB, LaneM, ThompsonJG (2008) Oocyte-secreted factors: regulators of cumulus cell function and oocyte quality. Hum Reprod Update 14: 159–177.

3. SuYQ, SugiuraK, EppigJJ (2009) Mouse oocyte control of granulosa cell development and function: paracrine regulation of cumulus cell metabolism. Semin Reprod Med 27: 32–42.

4. DongJ, AlbertiniDF, NishimoriK, KumarTR, LuN, et al. (1996) Growth differentiation factor-9 is required during early ovarian folliculogenesis. Nature 383: 531–535.

5. NilssonEE, SkinnerMK (2002) Growth and differentiation factor-9 stimulates progression of early primary but not primordial rat ovarian follicle development. Biol Reprod 67: 1018–1024.

6. GilchristRB, RitterLJ, MyllymaaS, Kaivo-OjaN, DragovicRA, et al. (2006) Molecular basis of oocyte-paracrine signalling that promotes granulosa cell proliferation. J Cell Sci 119: 3811–3821.

7. SpicerLJ, AadPY, AllenD, MazerbourgS, HsuehAJ (2006) Growth differentiation factor-9 has divergent effects on proliferation and steroidogenesis of bovine granulosa cells. J Endocrinol 189: 329–339.

8. HusseinTS, FroilandDA, AmatoF, ThompsonJG, GilchristRB (2005) Oocytes prevent cumulus cell apoptosis by maintaining a morphogenic paracrine gradient of bone morphogenetic proteins. J Cell Sci 118: 5257–5268.

9. OrisakaM, OrisakaS, JiangJY, CraigJ, WangY, et al. (2006) Growth differentiation factor 9 is antiapoptotic during follicular development from preantral to early antral stage. Mol Endocrinol 20: 2456–2468.

10. JuengelJL, BodensteinerKJ, HeathDA, HudsonNL, MoellerCL, et al. (2004) Physiology of GDF9 and BMP15 signalling molecules. Anim Reprod Sci 82–83: 447–460.

11. InagakiK, ShimasakiS (2010) Impaired production of BMP-15 and GDF-9 mature proteins derived from proproteins WITH mutations in the proregion. Mol Cell Endocrinol 328: 1–7.

12. OtsukaF, McTavishKJ, ShimasakiS (2011) Integral role of GDF-9 and BMP-15 in ovarian function. Mol Reprod Dev 78: 9–21.

13. GallowaySM, McNattyKP, CambridgeLM, LaitinenMP, JuengelJL, et al. (2000) Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner. Nat Genet 25: 279–283.

14. HanrahanJP, GreganSM, MulsantP, MullenM, DavisGH, et al. (2004) Mutations in the genes for oocyte-derived growth factors GDF9 and BMP15 are associated with both increased ovulation rate and sterility in Cambridge and Belclare sheep (Ovis aries). Biol Reprod 70: 900–909.

15. BodinL, Di PasqualeE, FabreS, BontouxM, MongetP, et al. (2007) A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep. Endocrinology 148: 393–400.

16. Martinez-RoyoA, JuradoJJ, SmuldersJP, MartiJI, AlabartJL, et al. (2008) A deletion in the bone morphogenetic protein 15 gene causes sterility and increased prolificacy in Rasa Aragonesa sheep. Anim Genet 39: 294–297.

17. MonteagudoLV, PonzR, TejedorMT, LavinaA, SierraI (2009) A 17 bp deletion in the Bone Morphogenetic Protein 15 (BMP15) gene is associated to increased prolificacy in the Rasa Aragonesa sheep breed. Anim Reprod Sci 110: 139–146.

18. MulsantP, LecerfF, FabreS, SchiblerL, MongetP, et al. (2001) Mutation in bone morphogenetic protein receptor-IB is associated with increased ovulation rate in Booroola Merino ewes. Proc Natl Acad Sci U S A 98: 5104–5109.

19. SouzaCJ, MacDougallC, CampbellBK, McNeillyAS, BairdDT (2001) The Booroola (FecB) phenotype is associated with a mutation in the bone morphogenetic receptor type 1 B (BMPR1B) gene. J Endocrinol 169: R1–6.

20. WilsonT, WuXY, JuengelJL, RossIK, LumsdenJM, et al. (2001) Highly prolific Booroola sheep have a mutation in the intracellular kinase domain of bone morphogenetic protein IB receptor (ALK-6) that is expressed in both oocytes and granulosa cells. Biol Reprod 64: 1225–1235.

21. NicolL, BishopSC, Pong-WongR, BendixenC, HolmLE, et al. (2009) Homozygosity for a single base-pair mutation in the oocyte-specific GDF9 gene results in sterility in Thoka sheep. Reproduction 138: 921–933.

22. SilvaBD, CastroEA, SouzaCJ, PaivaSR, SartoriR, et al. (2011) A new polymorphism in the Growth and Differentiation Factor 9 (GDF9) gene is associated with increased ovulation rate and prolificacy in homozygous sheep. Anim Genet 42: 89–92.

23. DixitH, RaoLK, PadmalathaV, KanakavalliM, DeenadayalM, et al. (2005) Mutational screening of the coding region of growth differentiation factor 9 gene in Indian women with ovarian failure. Menopause 12: 749–754.

24. LaissueP, Christin-MaitreS, TouraineP, KuttennF, RitvosO, et al. (2006) Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. Eur J Endocrinol 154: 739–744.

25. KovanciE, RohozinskiJ, SimpsonJL, HeardMJ, BishopCE, et al. (2007) Growth differentiating factor-9 mutations may be associated with premature ovarian failure. Fertil Steril 87: 143–146.

26. MontgomeryGW, ZhaoZZ, MarshAJ, MayneR, TreloarSA, et al. (2004) A deletion mutation in GDF9 in sisters with spontaneous DZ twins. Twin Res 7: 548–555.

27. PalmerJS, ZhaoZZ, HoekstraC, HaywardNK, WebbPM, et al. (2006) Novel variants in growth differentiation factor 9 in mothers of dizygotic twins. J Clin Endocrinol Metab 91: 4713–4716.

28. ZhaoH, QinY, KovanciE, SimpsonJL, ChenZJ, et al. (2007) Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure. Fertil Steril 88: 1474–1476.

29. Di PasqualeE, Beck-PeccozP, PersaniL (2004) Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene. Am J Hum Genet 75: 106–111.

30. Di PasqualeE, RossettiR, MarozziA, BodegaB, BorgatoS, et al. (2006) Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure. J Clin Endocrinol Metab 91: 1976–1979.

31. DixitH, RaoLK, PadmalathaVV, KanakavalliM, DeenadayalM, et al. (2006) Missense mutations in the BMP15 gene are associated with ovarian failure. Hum Genet 119: 408–415.

32. RossettiR, Di PasqualeE, MarozziA, BioneS, TonioloD, et al. (2009) BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein. Hum Mutat 30: 804–810.

33. HanevikHI, HilmarsenHT, SkjelbredCF, TanboT, KahnJA (2011) A single nucleotide polymorphism in BMP15 is associated with high response to ovarian stimulation. Reprod Biomed Online 23: 97–104.

34. MoronFJ, de CastroF, RoyoJL, MontoroL, MiraE, et al. (2006) Bone morphogenetic protein 15 (BMP15) alleles predict over-response to recombinant follicle stimulation hormone and iatrogenic ovarian hyperstimulation syndrome (OHSS). Pharmacogenet Genomics 16: 485–495.

35. YoshinoO, McMahonHE, SharmaS, ShimasakiS (2006) A unique preovulatory expression pattern plays a key role in the physiological functions of BMP-15 in the mouse. Proc Natl Acad Sci U S A 103: 10678–10683.

36. DavisGH (2005) Major genes affecting ovulation rate in sheep. Genet Sel Evol 37 Suppl 1: S11–23.

37. DavisGH, GallowaySM, RossIK, GreganSM, WardJ, et al. (2002) DNA tests in prolific sheep from eight countries provide new evidence on origin of the Booroola (FecB) mutation. Biol Reprod 66: 1869–1874.

38. VinetA, DrouilhetL, BodinL, MulsantP, FabreS, et al. (2012) Genetic control of multiple births in low ovulating mammalian species. Mamm Genome 23(11–12): 727–40.

39. PersaniL, RossettiR, CacciatoreC, FabreS (2011) Genetic defects of ovarian TGF-beta-like factors and premature ovarian failure. J Endocrinol Invest 34: 244–251.

40. FabreS, PierreA, MulsantP, BodinL, Di PasqualeE, et al. (2006) Regulation of ovulation rate in mammals: contribution of sheep genetic models. Reprod Biol Endocrinol 4: 20.

41. LiaoWX, MooreRK, ShimasakiS (2004) Functional and molecular characterization of naturally occurring mutations in the oocyte-secreted factors bone morphogenetic protein-15 and growth and differentiation factor-9. J Biol Chem 279: 17391–17396.

42. LiaoWX, MooreRK, OtsukaF, ShimasakiS (2003) Effect of intracellular interactions on the processing and secretion of bone morphogenetic protein-15 (BMP-15) and growth and differentiation factor-9. Implication of the aberrant ovarian phenotype of BMP-15 mutant sheep. J Biol Chem 278: 3713–3719.

43. McIntoshCJ, LunS, LawrenceS, WesternAH, McNattyKP, et al. (2008) The proregion of mouse BMP15 regulates the cooperative interactions of BMP15 and GDF9. Biol Reprod 79: 889–896.

44. McNattyKP, JuengelJL, ReaderKL, LunS, MyllymaaS, et al. (2005) Bone morphogenetic protein 15 and growth differentiation factor 9 co-operate to regulate granulosa cell function. Reproduction 129: 473–480.

45. EdwardsSJ, ReaderKL, LunS, WesternA, LawrenceS, et al. (2008) The cooperative effect of growth and differentiation factor-9 and bone morphogenetic protein (BMP)-15 on granulosa cell function is modulated primarily through BMP receptor II. Endocrinology 149: 1026–1030.

46. ReaderKL, HeathDA, LunS, McIntoshCJ, WesternAH, et al. (2011) Signalling pathways involved in the cooperative effects of ovine and murine GDF9+BMP15-stimulated thymidine uptake by rat granulosa cells. Reproduction 142: 123–131.

47. MooreRK, OtsukaF, ShimasakiS (2003) Molecular basis of bone morphogenetic protein-15 signaling in granulosa cells. J Biol Chem 278: 304–310.

48. VittUA, MazerbourgS, KleinC, HsuehAJ (2002) Bone morphogenetic protein receptor type II is a receptor for growth differentiation factor-9. Biol Reprod 67: 473–480.

49. MazerbourgS, KleinC, RohJ, Kaivo-OjaN, MottersheadDG, et al. (2004) Growth differentiation factor-9 signaling is mediated by the type I receptor, activin receptor-like kinase 5. Mol Endocrinol 18: 653–665.

50. FabreS, PierreA, PisseletC, MulsantP, LecerfF, et al. (2003) The Booroola mutation in sheep is associated with an alteration of the bone morphogenetic protein receptor-IB functionality. J Endocrinol 177: 435–444.

51. StephensM, SmithNJ, DonnellyP (2001) A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 68: 978–989.

52. StephensM, DonnellyP (2003) A comparison of bayesian methods for haplotype reconstruction from population genotype data. Am J Hum Genet 73: 1162–1169.

53. BaldingDJ (2006) A tutorial on statistical methods for population association studies. Nat Rev Genet 7: 781–791.

54. PurcellS, NealeB, Todd-BrownK, ThomasL, FerreiraMA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559–575.

55. SchaidDJ, RowlandCM, TinesDE, JacobsonRM, PolandGA (2002) Score tests for association between traits and haplotypes when linkage phase is ambiguous. Am J Hum Genet 70: 425–434.

56. ZaykinDV, WestfallPH, YoungSS, KarnoubMA, WagnerMJ, et al. (2002) Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals. Hum Hered 53: 79–91.

57. KyteJ, DoolittleRF (1982) A simple method for displaying the hydropathic character of a protein. J Mol Biol 157: 105–132.

58. ZimmermanJM, EliezerN, SimhaR (1968) The characterization of amino acid sequences in proteins by statistical methods. J Theor Biol 21: 170–201.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 4
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#