Pivotal role of the muscle-contraction pathway in cryptorchidism and evidence for genomic connections with cardiomyopathy pathways in RASopathies
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  • 作者:Carlo V Cannistraci (1) (2) (3)
    Jernej Ogorevc (4)
    Minja Zorc (4)
    Timothy Ravasi (1)
    Peter Dovc (4)
    Tanja Kunej (4)
  • 关键词:Cryptorchidism ; Muscle ; contraction pathway ; Cardiomyopathy ; Comparative integratomics ; Protein ; protein interactions ; Systems biology ; Undescended testes ; RASopathy
  • 刊名:BMC Medical Genomics
  • 出版年:2013
  • 出版时间:December 2013
  • 年:2013
  • 卷:6
  • 期:1
  • 全文大小:2069KB
  • 参考文献:1. Dovc P, Kunej T, Williams GA: Genetics and genomics of reproductive disorders. In / Reproductive Genomics of Domestic Animals. 1st edition. Edited by: Jiang Z, Ott TL. Oxford, UK: Wiley-Blackwell; 2010:67鈥?7. CrossRef
    2. Amann RP, Veeramachaneni DNR: Cryptorchidism in common eutherian mammals. / Reproduction 2007,133(3):541鈥?61. CrossRef
    3. Foresta C, Zuccarello D, Garolla A, Ferlin A: Role of hormones, genes, and environment in human cryptorchidism. / Endocr Rev 2008,29(5):560鈥?80. CrossRef
    4. Barthold JS: Undescended testis: current theories of etiology. / Curr Opin Urol 2008,18(4):395鈥?00. CrossRef
    5. Mortell A, Montedonico S, Puri P: Animal models in pediatric surgery. / Pediatr Surg Int 2006,22(2):111鈥?28. CrossRef
    6. Oti M, Huynen MA, Brunner HG: Phenome connections. / Trends Genet 2008,24(3):103鈥?06. CrossRef
    7. Barthold JS, McCahan SM, Singh AV, Knudsen TB, Si X, Campion L, Akins RE: Altered expression of muscle- and cytoskeleton-related genes in a rat strain with inherited cryptorchidism. / J Androl 2008,29(3):352鈥?66. CrossRef
    8. Ogorevc J, Kunej T, Razpet A, Dovc P: Database of cattle candidate genes and genetic markers for milk production and mastitis. / Anim Genet 2009,40(6):832鈥?51. CrossRef
    9. Ogorevc J, Dovc P, Kunej T: Comparative genomics approach to identify candidate genetic loci for male fertility. / Reprod Domest Anim 2011,46(2):229鈥?39. CrossRef
    10. Kunej T, Jevsinek Skok D, Zorc M, Ogrinc A, Michal JJ, Kovac M, Jiang Z: Obesity gene atlas in mammals. / J Genomics 2012, 1:45鈥?5.
    11. Moreau Y, Tranchevent LC: Computational tools for prioritizing candidate genes: boosting disease gene discovery. / Nat Rev Genet 2012,13(8):523鈥?36. CrossRef
    12. Zorc M, Jevsinek Skok D, Godnic I, Calin GA, Horvat S, Jiang Z, Dovc P, Kunej T: Catalog of MicroRNA Seed Polymorphisms in Vertebrates. / PLoS One 2012,7(1):e30737. CrossRef
    13. da Huang W, Sherman BT, Tan Q, Kir J, Liu D, Bryant D, Guo Y, Stephens R, Baseler MW, Lane HC: DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists. / Nucleic Acids Res 2007,35(Web Server issue):W169-W175. CrossRef
    14. Razick S, Magklaras G, Donaldson IM: iRefIndex: a consolidated protein interaction database with provenance. / BMC Bioinforma 2008, 9:405. CrossRef
    15. Chuang HY, Lee E, Liu YT, Lee D, Ideker T: Network-based classification of breast cancer metastasis. / Mol Syst Biol 2007, 3:140. CrossRef
    16. Ravasi T, Cannistraci CV, Suzuki H, Katayama S, Bajic VB, Tan K, Akalin A, Schmeier S, Kanamori-Katayama M, Bertin N: An Atlas of Combinatorial Transcriptional Regulation in Mouse and Man. / Cell 2010,140(5):744鈥?52. CrossRef
    17. Kamburov A, Wierling C, Lehrach H, Herwig R: ConsensusPathDB--a database for integrating human functional interaction networks. / Nucleic Acids Res 2009,37(Database issue):D623-D628. CrossRef
    18. Smoot M, Ono K, Ideker T, Maere S: PiNGO: a Cytoscape plugin to find candidate genes in biological networks. / Bioinformatics 2011,27(7):1030鈥?031. CrossRef
    19. Smoot ME, Ono K, Ruscheinski J, Wang PL, Ideker T: Cytoscape 2.8: new features for data integration and network visualization. / Bioinformatics 2011,27(3):431鈥?32. CrossRef
    20. Szklarczyk D, Franceschini A, Kuhn M, Simonovic M, Roth A, Minguez P, Doerks T, Stark M, Muller J, Bork P: The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored. / Nucleic Acids Res 2011,39(Database issue):D561-D568. CrossRef
    21. Hiard S, Charlier C, Coppieters W, Georges M, Baurain D: Patrocles: a database of polymorphic miRNA-mediated gene regulation in vertebrates. / Nucleic Acids Res 2010,38(Database issue):D640-D651. CrossRef
    22. Miyake Y, Kaneda Y: A new type of Robertsonian translocation (1/26) in a bull with unilateral cryptorchidism, probably occurring de novo. / Nihon juigaku zasshi J Vet Sci 1987,49(6):1015鈥?019. CrossRef
    23. Sasagawa I, Nakada T, Ishigooka M, Sawamura T, Adachi Y, Hashimoto T: Chromosomal anomalies in cryptorchidism. / Int Urol Nephrol 1996,28(1):99鈥?02. CrossRef
    24. Ogata T, Muroya K, Matsuo N, Hata J, Fukushima Y, Suzuki Y: Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p. / J Med Genet 1997,34(4):331鈥?34. CrossRef
    25. Suzuki Y, Sasagawa I, Nakada T, Onmura Y: Bilateral cryptorchidism associated with terminal deletion of 10q. / Urol Int 1998,61(3):186鈥?87. CrossRef
    26. Goldschmidt B, El-Jaick KB, Souza LM, Carvalho ECQ, Moura VLS, Benevides Filho IM: Cryptorchidism associated with 78, XY/79, XXY mosaicism in dog. / Israel J Vet Med 2001, 56:56鈥?8.
    27. Moreno-Garcia M, Miranda EB: Chromosomal anomalies in cryptorchidism and hypospadias. / J Urol 2002,168(5):2170鈥?172. discussion 2172 CrossRef
    28. Prabhakara K, Angalena R, Ramadevi AR: Familial (9;11)(p22;p15.5)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development. / Genetic counseling (Geneva, Switzerland) 2004,15(1):37鈥?1.
    29. Brito L, Sertich PL, Durkin K, Chowdhary BP, Turner RM, Greene LM, McDonnell S: Autosomic 27 Trisomy in a Standardbred Colt. / J Equine Vet Sci 2008,28(7):431鈥?36. CrossRef
    30. Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J: A new look at XXYY syndrome: medical and psychological features. / Am J Med Genet A 2008,146A(12):1509鈥?522. CrossRef
    31. van der Veken LT, Dieleman MM, Douben H, van de Brug JC, van de Graaf R, Hoogeboom AJ, Poddighe PJ, de Klein A: Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies. / Mol Cytogenet 2010, 3:13. CrossRef
    32. Niyazov DM, Nawaz Z, Justice AN, Toriello HV, Martin CL, Adam MP: Genotype/phenotype correlations in two patients with 12q subtelomere deletions. / Am J Med Genet A 2007,143A(22):2700鈥?705. CrossRef
    33. Melis D, Genesio R, Boemio P, Del Giudice E, Cappuccio G, Mormile A, Ronga V, Conti A, Imperati F, Nitsch L: Clinical description of a patient carrying the smallest reported deletion involving 10p14 region. / Am J Med Genet A 2012,158A(4):832鈥?35. CrossRef
    34. Tannour-Louet M, Han S, Corbett ST, Louet JF, Yatsenko S, Meyers L, Shaw CA, Kang SH, Cheung SW, Lamb DJ: Identification of de novo copy number variants associated with human disorders of sexual development. / PLoS One 2010,5(10):e15392. CrossRef
    35. Peltonen L, Perola M, Naukkarinen J, Palotie A: Lessons from studying monogenic disease for common disease. / Hum Mol Genet 2006, 15:R67-R74. Spec No 1 CrossRef
    36. Gianotten J, van der Veen F, Alders M, Leschot NJ, Tanck MW, Land JA, Kremer JA, Hoefsloot LH, Mannens MM, Lombardi MP: Chromosomal region 11p15 is associated with male factor subfertility. / Mol Hum Reprod 2003,9(10):587鈥?92. CrossRef
    37. Klonisch T, Fowler PA, Hombach-Klonisch S: Molecular and genetic regulation of testis descent and external genitalia development. / Dev Biol 2004,270(1):1鈥?8. CrossRef
    38. Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R: WT-1 IS REQUIRED FOR EARLY KIDNEY DEVELOPMENT. / Cell 1993,74(4):679鈥?91. CrossRef
    39. Ikadai H, Ajisawa C, Taya K, Imamichi T: Suprainguinal ectopic scrota of TS inbred rats. / J Reprod Fertil 1988,84(2):701鈥?07. CrossRef
    40. Li X, Nokkala E, Yan W, Streng T, Saarinen N, Warri A, Huhtaniemi I, Santti R, Makela S, Poutanen M: Altered structure and function of reproductive organs in transgenic male mice overexpressing human aromatase. / Endocrinology 2001,142(6):2435鈥?442. CrossRef
    41. Caron P, Imbeaud S, Bennet A, Plantavid M, Camerino G, Rochiccioli P: Combined hypothalamic-pituitary-gonadal defect in a hypogonadic man with a novel mutation in the DAX-1 gene. / J Clin Endocrinol Metab 1999,84(10):3563鈥?569. CrossRef
    42. Donaldson KM, Tong SY, Washburn T, Lubahn DB, Eddy EM, Hutson JM, Korach KS: Morphometric study of the gubernaculum in male estrogen receptor mutant mice. / J Androl 1996,17(2):91鈥?5.
    43. Gorlov IP, Kamat A, Bogatcheva NV, Jones E, Lamb DJ, Truong A, Bishop CE, McElreavey K, Agoulnik AI: Mutations of the GREAT gene cause cryptorchidism. / Hum Mol Genet 2002,11(19):2309鈥?318. CrossRef
    44. Canto P, Escudero I, Soderlund D, Nishimura E, Carranza-Lira S, Gutierrez J, Nava A, Mendez JP: A novel mutation of the insulin-like 3 gene in patients with cryptorchidism. / J Hum Genet 2003,48(2):86鈥?0. CrossRef
    45. Ferlin A, Garolla A, Bettella A, Bartoloni L, Vinanzi C, Roverato A, Foresta C: Androgen receptor gene CAG and GGC repeat lengths in cryptorchidism. / Eur J Endocrinol 2005,152(3):419鈥?25. CrossRef
    46. Yoshida R, Fukami M, Sasagawa I, Hasegawa T, Kamatani N, Ogata T: Association of cryptorchidism with a specific haplotype of the estrogen receptor alpha gene: implication for the susceptibility to estrogenic environmental endocrine disruptors. / J Clin Endocrinol Metab 2005,90(8):4716鈥?721. CrossRef
    47. Ferlin A, Bogatcheva NV, Gianesello L, Pepe A, Vinanzi C, Agoulnik AI, Foresta C: Insulin-like factor 3 gene mutations in testicular dysgenesis syndrome: clinical and functional characterization. / Mol Hum Reprod 2006,12(6):401鈥?06. CrossRef
    48. Silva-Ramos M, Oliveira JM, Cabeda JM, Reis A, Soares J, Pimenta A: The CAG repeat within the androgen receptor gene and its relationship to cryptorchidism. / Int Braz J Urol 2006,32(3):330鈥?34. discussion 335 CrossRef
    49. Wada Y, Okada M, Fukami M, Sasagawa I, Ogata T: Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1. / Fertil Steril 2006,85(3):787鈥?90. CrossRef
    50. Bogatcheva NV, Ferlin A, Feng S, Truong A, Gianesello L, Foresta C, Agoulnik AI: T222P mutation of the insulin-like 3 hormone receptor LGR8 is associated with testicular maldescent and hinders receptor expression on the cell surface membrane. / Am J Physiol Endocrinol Metab 2007,292(1):E138-E144. CrossRef
    51. El Houate B, Rouba H, Sibai H, Barakat A, Chafik A, Chadli el B, Imken L, Bogatcheva NV, Feng S, Agoulnik AI: Novel mutations involving the INSL3 gene associated with cryptorchidism. / J Urol 2007,177(5):1947鈥?951. CrossRef
    52. Yamazawa K, Wada Y, Sasagawa I, Aoki K, Ueoka K, Ogata T: Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism. / Horm Res 2007,67(2):73鈥?6. CrossRef
    53. Wang Y, Barthold J, Figueroa E, Gonzalez R, Noh PH, Wang M, Manson J: Analysis of five single nucleotide polymorphisms in the ESR1 gene in cryptorchidism. / Birth Defects Res A Clin Mol Teratol 2008,82(6):482鈥?85. CrossRef
    54. Harris RM, Finlayson C, Weiss J, Fisher L, Hurley L, Barrett T, Emge D, Bathgate RA, Agoulnik AI, Jameson JL: A missense mutation in LRR8 of RXFP2 is associated with cryptorchidism. / Mamm Genome 2010,21(9鈥?0):442鈥?49. CrossRef
    55. Tang KF, Zheng JZ, Xing JP: Molecular analysis of SNP12 in estrogen receptor alpha gene in hypospadiac or cryptorchid patients from Northwestern China. / Urol Int 2011,87(3):359鈥?62. CrossRef
    56. Feng S, Ferlin A, Truong A, Bathgate R, Wade JD, Corbett S, Han S, Tannour-Louet M, Lamb DJ, Foresta C: INSL3/RXFP2 signaling in testicular descent. / Ann N Y Acad Sci 2009, 1160:197鈥?04. CrossRef
    57. Dalgaard MD, Weinhold N, Edsgard D, Silver JD, Pers TH, Nielsen JE, Jorgensen N, Juul A, Gerds TA, Giwercman A: A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation. / J Med Genet 2012,49(1):58鈥?5. CrossRef
    58. Kolon TF, Wiener JS, Lewitton M, Roth DR, Gonzales ET Jr, Lamb DJ: Analysis of homeobox gene HOXA10 mutations in cryptorchidism. / J Urol 1999,161(1):275鈥?80. CrossRef
    59. Teles MG, Trarbach EB, Noel SD, Guerra-Junior G, Jorge A, Beneduzzi D, Bianco SD, Mukherjee A, Baptista MT, Costa EM: A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. / Eur J Endocrinol 2010,163(1):29鈥?4. CrossRef
    60. Williams GA, Ott TL, Michal JJ, Gaskins CT, Wright RW Jr, Daniels TF, Jiang Z: Development of a model for mapping cryptorchidism in sheep and initial evidence for association of INSL3 with the defect. / Anim Genet 2007,38(2):189鈥?91. CrossRef
    61. Cassata R, Iannuzzi A, Parma P, De Lorenzi L, Peretti V, Perucatti A, Iannuzzi L, Di Meo GP: Clinical, cytogenetic and molecular evaluation in a dog with bilateral cryptorchidism and hypospadias. / Cytogenet Genome Res 2008,120(1鈥?):140鈥?43. CrossRef
    62. Zhao X, Du ZQ, Rothschild MF: An association study of 20 candidate genes with cryptorchidism in Siberian Husky dogs. / J Anim Breed Genet 2010,127(4):327鈥?31. CrossRef
    63. Galan JJ, Guarducci E, Nuti F, Gonzalez A, Ruiz M, Ruiz A, Krausz C: Molecular analysis of estrogen receptor alpha gene AGATA haplotype and SNP12 in European populations: potential protective effect for cryptorchidism and lack of association with male infertility. / Hum Reprod 2007,22(2):444鈥?49. CrossRef
    64. Pathirana IN, Tanaka K, Kawate N, Tsuji M, Kida K, Hatoya S, Inaba T, Tamada H: Analysis of single nucleotide polymorphisms in the 3鈥?region of the estrogen receptor 1 gene in normal and cryptorchid Miniature Dachshunds and Chihuahuas. / J Reprod Dev 2010,56(4):405鈥?10. CrossRef
    65. Lo Giacco D, Ars E, Bassas L, Galan JJ, Rajmil O, Ruiz P, Caffaratti J, Guarducci E, Ruiz-Castane E, Krausz C: ESR1 promoter polymorphism is not associated with nonsyndromic cryptorchidism. / Fertil Steril 2011,95(1):369鈥?71. 371 e361鈥?62 CrossRef
    66. Krausz C, Quintana-Murci L, Fellous M, Siffroi JP, McElreavey K: Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism. / Mol Hum Reprod 2000,6(4):298鈥?02. CrossRef
    67. Takahashi I, Takahashi T, Komatsu M, Matsuda J, Takada G: Ala/Thr60 variant of the Leydig insulin-like hormone is not associated with cryptorchidism in the Japanese population. / Pediatr Int 2001,43(3):256鈥?58. CrossRef
    68. Baker LA, Nef S, Nguyen MT, Stapleton R, Nordenskjold A, Pohl H, Parada LF: The insulin-3 gene: lack of a genetic basis for human cryptorchidism. / J Urol 2002,167(6):2534鈥?537. CrossRef
    69. Bertini V, Bertelloni S, Valetto A, Lala R, Foresta C, Simi P: Homeobox HOXA10 gene analysis in cryptorchidism. / J Pediatr Endocrinol Metab 2004,17(1):41鈥?5. CrossRef
    70. Nuti F, Marinari E, Erdei E, El-Hamshari M, Echavarria MG, Ars E, Balercia G, Merksz M, Giachini C, Shaeer KZ: The leucine-rich repeat-containing G protein-coupled receptor 8 gene T222P mutation does not cause cryptorchidism. / J Clin Endocrinol Metab 2008,93(3):1072鈥?076. CrossRef
    71. Simoni M, Tuttelmann F, Michel C, Bockenfeld Y, Nieschlag E, Gromoll J: Polymorphisms of the luteinizing hormone/chorionic gonadotropin receptor gene: association with maldescended testes and male infertility. / Pharmacogenet Genomics 2008,18(3):193鈥?00. CrossRef
    72. Kunej T, Zorn B, Peterlin B: Y chromosome microdeletions in infertile men with cryptorchidism. / Fertil Steril 2003,79(Suppl 3):1559鈥?565. CrossRef
    73. Bor P, Hindkjaer J, Kolvraa S, Rossen P, von der Maase H, Jorgensen TM, Sorensen VT, Eiberg H, Ingerslev HJ: Screening for Y microdeletions in men with testicular cancer and undescended testis. / J Assist Reprod Genet 2006,23(1):41鈥?5. CrossRef
    74. Gurbuz N, Ozbay B, Aras B, Tasci AI: Do microdeletions in the AZF region of the Y chromosome accompany cryptorchidism in Turkish children? / Int Urol Nephrol 2008,40(3):577鈥?81. CrossRef
    75. Hejmej A, Gorazd M, Kosiniak-Kamysz K, Wiszniewska B, Sadowska J, Bilinska B: Expression of aromatase and oestrogen receptors in reproductive tissues of the stallion and a single cryptorchid visualised by means of immunohistochemistry. / Domest Anim Endocrinol 2005,29(3):534鈥?47. CrossRef
    76. Nguyen MT, Delaney DP, Kolon TF: Gene expression alterations in cryptorchid males using spermatozoal microarray analysis. / Fertil Steril 2009,92(1):182鈥?87. CrossRef
    77. Hutson JM, Watts LM, Farmer PJ: Congenital undescended testes in neonatal pigs and the effect of exogenous calcitonin gene-related peptide. / J Urol 1998,159(3):1025鈥?028. CrossRef
    78. Zuccarello D, Morini E, Douzgou S, Ferlin A, Pizzuti A, Salpietro DC, Foresta C, Dallapiccola B: Preliminary data suggest that mutations in the CgRP pathway are not involved in human sporadic cryptorchidism. / J Endocrinol Invest 2004,27(8):760鈥?64.
    79. Bertola DR, Pereira AC, Passetti F, de Oliveira PS, Messiaen L, Gelb BD, Kim CA, Krieger JE: Neurofibromatosis-Noonan syndrome: molecular evidence of the concurrence of both disorders in a patient. / Am J Med Genet A 2005,136(3):242鈥?45.
    80. Digilio MC, Lepri F, Baban A, Dentici ML, Versacci P, Capolino R, Ferese R, De Luca A, Tartaglia M, Marino B: RASopathies: Clinical Diagnosis in the First Year of Life. / Molecular syndromology 2011,1(6):282鈥?89. CrossRef
    81. Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG: Germline gain-of-function mutations in SOS1 cause Noonan syndrome. / Nat Genet 2007,39(1):70鈥?4. CrossRef
    82. Razzaque MA, Nishizawa T, Komoike Y, Yagi H, Furutani M, Amo R, Kamisago M, Momma K, Katayama H, Nakagawa M: Germline gain-of-function mutations in RAF1 cause Noonan syndrome. / Nat Genet 2007,39(8):1013鈥?017. CrossRef
    83. Cannistraci CV, Ravasi T, Montevecchi FM, Ideker T, Alessio M: Nonlinear dimension reduction and clustering by Minimum Curvilinearity unfold neuropathic pain and tissue embryological classes. / Bioinformatics 2010,26(18):i531-i539. CrossRef
    84. Navlakha S, Kingsford C: The power of protein interaction networks for associating genes with diseases. / Bioinformatics (Oxford, England) 2010, 26:1057鈥?063. England CrossRef
    85. Rzhetsky A, Wajngurt D, Park N, Zheng T: Probing genetic overlap among complex human phenotypes. / P Natl Acad Sci USA 2007,104(28):11694鈥?1699. CrossRef
    86. Wu X, Jiang R, Zhang MQ, Li S: Network-based global inference of human disease genes. / Mol Syst Biol 2008, 4:189. CrossRef
    87. Wu X, Liu Q, Jiang R: Align human interactome with phenome to identify causative genes and networks underlying disease families. / Bioinformatics 2009,25(1):98鈥?04. CrossRef
    88. Loscalzo J, Barabasi AL: Systems biology and the future of medicine. / Wiley Interdiscip Rev Syst Biol Med 2011,3(6):619鈥?27. CrossRef
    89. Oti M, Brunner HG: The modular nature of genetic diseases. / Clin Genet 2007,71(1):1鈥?1. CrossRef
    90. Ogorevc J, Dovc P, Kunej T: Polymorphisms in microRNA targets: a source of new molecular markers for male reproduction. / Asian J Androl 2011,13(3):505鈥?08. CrossRef
    91. Kunej T, Skok DJ, Horvat S, Dovc P, Jiang Z: The glypican 3-hosted murine mir717 gene: sequence conservation, seed region polymorphisms and putative targets. / Int J Biol Sci 2010,6(7):769鈥?72. CrossRef
    92. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1755-8794/6/5/prepub
  • 作者单位:Carlo V Cannistraci (1) (2) (3)
    Jernej Ogorevc (4)
    Minja Zorc (4)
    Timothy Ravasi (1)
    Peter Dovc (4)
    Tanja Kunej (4)

    1. Integrative Systems Biology Laboratory, Biological and Environmental Sciences and Engineering Division, Computer, Electrical and Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University for Science and Technology (KAUST), Thuwal, Saudi Arabia
    2. Department of Mechanics, Politecnico di Torino, Turin, Italy
    3. Proteome Biochemistry Unit, San Raffaele Scientific Institute, Milan, Italy
    4. Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Domzale, Slovenia
  • ISSN:1755-8794
文摘
Background Cryptorchidism is the most frequent congenital disorder in male children; however the genetic causes of cryptorchidism remain poorly investigated. Comparative integratomics combined with systems biology approach was employed to elucidate genetic factors and molecular pathways underlying testis descent. Methods Literature mining was performed to collect genomic loci associated with cryptorchidism in seven mammalian species. Information regarding the collected candidate genes was stored in MySQL relational database. Genomic view of the loci was presented using Flash GViewer web tool (http://gmod.org/wiki/Flashgviewer/). DAVID Bioinformatics Resources 6.7 was used for pathway enrichment analysis. Cytoscape plug-in PiNGO 1.11 was employed for protein-network-based prediction of novel candidate genes. Relevant protein-protein interactions were confirmed and visualized using the STRING database (version 9.0). Results The developed cryptorchidism gene atlas includes 217 candidate loci (genes, regions involved in chromosomal mutations, and copy number variations) identified at the genomic, transcriptomic, and proteomic level. Human orthologs of the collected candidate loci were presented using a genomic map viewer. The cryptorchidism gene atlas is freely available online: http://www.integratomics-time.com/cryptorchidism/. Pathway analysis suggested the presence of twelve enriched pathways associated with the list of 179 literature-derived candidate genes. Additionally, a list of 43 network-predicted novel candidate genes was significantly associated with four enriched pathways. Joint pathway analysis of the collected and predicted candidate genes revealed the pivotal importance of the muscle-contraction pathway in cryptorchidism and evidence for genomic associations with cardiomyopathy pathways in RASopathies. Conclusions The developed gene atlas represents an important resource for the scientific community researching genetics of cryptorchidism. The collected data will further facilitate development of novel genetic markers and could be of interest for functional studies in animals and human. The proposed network-based systems biology approach elucidates molecular mechanisms underlying co-presence of cryptorchidism and cardiomyopathy in RASopathies. Such approach could also aid in molecular explanation of co-presence of diverse and apparently unrelated clinical manifestations in other syndromes.

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