Electrophoretic Techniques for the Detection of Human Microsatellite D19S884.

作者: Fazliana Mansor , Siti Sarah Hamzah , Liyana Zamri

DOI:

关键词:

摘要: Background The detection and analysis of microsatellites is very important for the mapping genetic diseases because they are commonly used as markers. Microsatellite marker D19S884 has been associated with polycystic ovary syndrome (PCOS), most common reproductive endocrine disease women in their childbearing years. It responsible an estimated 70% cases anovulatory infertility. In this work, we detected DNA extracted from blood PCOS patients. Methods were amplified by polymerase chain reaction (PCR) using a pair specific primers tagged fluorescence to yield products 160-200 base pairs length. Alleles separated on 4% low-melting agarose gels; stained safe gel staining, GelRed™, which alternative ethidium bromide; visualised ultraviolet illumination. Results Bands observed, but base-pairs differences difficult distinguish. To identify each allele clearly, PCR also analysed capillary electrophoresis fragment where it was possible discriminate even case difference between two bases alleles. Conclusion article, present protocol that combines use identification biomarkers PCOS.

参考文章(17)
Rong Mao, Pinar Bayrak-Toydemir, Elaine Lyon, Capillary Electrophoresis for the Detection of Fragile X Expanded Alleles Methods in Molecular Biology. ,vol. 919, pp. 275- 285 ,(2013) , 10.1007/978-1-62703-029-8_24
Masakazu Inazuka, Hans-Michael Wenz, Munechika Sakabe, Tomoko Tahira, Kenshi Hayashi, A Streamlined Mutation Detection System: Multicolor Post-PCR Fluorescence Labeling and Single-Strand Conformational Polymorphism Analysis by Capillary Electrophoresis Genome Research. ,vol. 7, pp. 1094- 1103 ,(1997) , 10.1101/GR.7.11.1094
M. Urbanek, R. S. Legro, D. A. Driscoll, R. Azziz, D. A. Ehrmann, R. J. Norman, J. F. Strauss, R. S. Spielman, A. Dunaif, THIRTY-SEVEN CANDIDATE GENES FOR POLYCYSTIC OVARY SYNDROME : STRONGEST EVIDENCE FOR LINKAGE IS WITH FOLLISTATIN Proceedings of the National Academy of Sciences of the United States of America. ,vol. 96, pp. 8573- 8578 ,(1999) , 10.1073/PNAS.96.15.8573
Kathryn G. Ewens, Douglas R. Stewart, Wendy Ankener, Margrit Urbanek, Jan M. McAllister, Chen Chen, K. Maravet Baig, Stephen C. J. Parker, Elliot H. Margulies, Richard S. Legro, Andrea Dunaif, Jerome F. Strauss, Richard S. Spielman, Family-based analysis of candidate genes for polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. ,vol. 95, pp. 2306- 2315 ,(2010) , 10.1210/JC.2009-2703
Stephen Franks, Mark McCarthy, Genetics of Ovarian Disorders: Polycystic Ovary Syndrome Reviews in Endocrine and Metabolic Disorders. ,vol. 5, pp. 69- 76 ,(2004) , 10.1023/B:REMD.0000016125.05878.96
K Moazami-Goudarzi, J P Furet, F Grosclaude, D Laloë, Analysis of genetic relationships between 10 cattle breeds with 17 microsatellites Animal Genetics. ,vol. 28, pp. 338- 345 ,(1997) , 10.1111/J.1365-2052.1997.00176.X
I. Martín-Burriel, E. García-Muro, P. Zaragoza, GENETIC DIVERSITY ANALYSIS OF SIX SPANISH NATIVE CATTLE BREEDS USING MICROSATELLITES Animal Genetics. ,vol. 30, pp. 177- 182 ,(1999) , 10.1046/J.1365-2052.1999.00437.X
S. Franks, N. Gharani, D. Waterworth, S. Batty, D. White, R. Williamson, M. McCarthy, The genetic basis of polycystic ovary syndrome. Human Reproduction. ,vol. 12, pp. 2641- 2648 ,(1997) , 10.1093/HUMREP/12.12.2641
Theo Vos, Abraham D Flaxman, Mohsen Naghavi, Rafael Lozano, Catherine Michaud, Majid Ezzati, Kenji Shibuya, Joshua A Salomon, Safa Abdalla, Victor Aboyans, Jerry Abraham, Ilana Ackerman, Rakesh Aggarwal, Stephanie Y Ahn, Mohammed K Ali, Mohammad A AlMazroa, Miriam Alvarado, H Ross Anderson, Laurie M Anderson, Kathryn G Andrews, Charles Atkinson, Larry M Baddour, Adil N Bahalim, Suzanne Barker-Collo, Lope H Barrero, David H Bartels, Maria-Gloria Basáñez, Amanda Baxter, Michelle L Bell, Emelia J Benjamin, Derrick Bennett, Eduardo Bernabé, Kavi Bhalla, Bishal Bhandari, Boris Bikbov, Aref Bin Abdulhak, Gretchen Birbeck, James A Black, Hannah Blencowe, Jed D Blore, Fiona Blyth, Ian Bolliger, Audrey Bonaventure, Soufiane Boufous, Rupert Bourne, Michel Boussinesq, Tasanee Braithwaite, Carol Brayne, Lisa Bridgett, Simon Brooker, Peter Brooks, Traolach S Brugha, Claire Bryan-Hancock, Chiara Bucello, Rachelle Buchbinder, Geoffrey Buckle, Christine M Budke, Michael Burch, Peter Burney, Roy Burstein, Bianca Calabria, Benjamin Campbell, Charles E Canter, Hélène Carabin, Jonathan Carapetis, Loreto Carmona, Claudia Cella, Fiona Charlson, Honglei Chen, Andrew Tai-Ann Cheng, David Chou, Sumeet S Chugh, Luc E Coffeng, Steven D Colan, Samantha Colquhoun, K Ellicott Colson, John Condon, Myles D Connor, Leslie T Cooper, Matthew Corriere, Monica Cortinovis, Karen Courville De Vaccaro, William Couser, Benjamin C Cowie, Michael H Criqui, Marita Cross, Kaustubh C Dabhadkar, Manu Dahiya, Nabila Dahodwala, James Damsere-Derry, Goodarz Danaei, Adrian Davis, Diego De Leo, Louisa Degenhardt, Robert Dellavalle, Allyne Delossantos, Julie Denenberg, Sarah Derrett, Don C Des Jarlais, Samath D Dharmaratne, Mukesh Dherani, Cesar Diaz-Torne, Helen Dolk, E Ray Dorsey, Tim Driscoll, Herbert Duber, Beth Ebel, Karen Edmond, Alexis Elbaz, Suad Eltahir Ali, Holly Erskine, Patricia J Erwin, Patricia Espindola, Stalin E Ewoigbokhan, Farshad Farzadfar, Valery Feigin, David T Felson, Alize Ferrari, Cleusa P Ferri, Eric M Fèvre, Mariel M Finucane, Seth Flaxman, Louise Flood, Kyle Foreman, Mohammad H Forouzanfar, Francis Gerry R Fowkes, Richard Franklin, Marlene Fransen, Michael K Freeman, Belinda J Gabbe, Sherine E Gabriel, Emmanuela Gakidou, Hammad A Ganatra, Bianca Garcia, Flavio Gaspari, Richard F Gillum, Gerhard Gmel, Richard Gosselin, Rebecca Grainger, Justina Groeger, Francis Guillemin, David Gunnell, Ramyani Gupta, Juanita Haagsma, Holly Hagan, Yara A Halasa, Wayne Hall, Diana Haring, Josep Maria Haro, James E Harrison, None, Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010 The Lancet. ,vol. 380, pp. 2163- 2196 ,(2012) , 10.1016/S0140-6736(12)61729-2