2020, Number 3
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Rev Cub Gen 2020; 13 (3)
Dynamics of filial relationship studies in Cuba
Collazo MT, Hernández PY, Gómez MM, Juárez FR, Machado MD, Merencio SL, Ferreira CR
Language: Spanish
References: 24
Page: 1-20
PDF size: 796.59 Kb.
ABSTRACT
Introduction: Uncertainty about filial relationships has psico-social effects on people involved, and at present it is possible to be resolved using DNA markers. These kinds of studies are being developed since 2017 thanks to the collaboration between Cubans National Centre for Medical Genetics and Legal Medicine Institute.
Objectives: Knowing the main characteristics of filial relationships studies developed in Cuba during 2017 and 2018 in order to draw up an approach for long-term continuity.
Methods: One hundred relationship studies, involving 115 filial relationship analyses, were resolved using 11 STR tipe DNA markers, which were genotyped through Polymerase Chain Reaction, denaturant polyacrylamide gel electrophoresis and silver staining. The proposal goals were to obtain at least a Paterninity Index equal or higher than 100 or no less than 3 exclusions. Multiplex system GenomeLab™ Human STR Primer Set (Beckman Coulter) was used in some studies that not achieved closing parameters or where rare genetic events were presented.
Results: Paternity studies were 98 % of total. Other kinds of studies were maternity test and siblings test (one case each one). One hundred fifteen filial relationships were analyzed, 112 of them being paternity relationships. Paternity analysis including mother were 76.8 % of them. Paternity was excluded in 33 % of paternity analysis, being 4 the average number of exclusion markers. 96.4 % of paternity analysis matched quality parameters concerning close standards.
REFERENCES
Meerum Terwogt M, Meerum-Terwogt-Reijnders CJ, van Hekken SMJ. Identity problems related to an absent genetic father. Zeitschrift für Familienforschung. 2002 [acceso 22/06/2018];14,257-71. Disponible en: http://www.zeitschrift-fuer-familienforschung.de/pdf/2002-3-terwogt.pdf.
Björklund A, Eriksson KH, Sundström M. Children of unknown fathers: Prevalence and outcomes in Sweden. Swedish Institute for Social Research. StockholmUniversity. Working Paper 6/2011. Published in March 24,2011. [acceso 21/06/2019]; Disponible en: https://www.diva-portal.org/smash/get/ diva2:407290/FULLTEXT01.pdf
Organización Mundial de la Salud (2006). Constitución de la OMS: Documentos básicos, suplemento de la 45ª edición, octubre de 2006. Disponible en: https://www.who.int/governance/eb/who_constitution_en.pdf
Landsteiner, K. Zur Kenntnis der antifermentativen, lytisichen und agglutinierenden Wirkungen des Blutserums und der Lymphe. Zentralbl. Bakteriol.1900; 27,357–62.
Jeffreys AJ, Wilson V, Neumann R y Keyte J. Amplification of human niinisatellites by the polymerase chain reaction: towards DNA flgerprinting of single cells. Nucleic Acids Res;1988:16(23):10953-71.
Foreman LA, Champod C, Evett IW, Lambert JA, Pope S. Interpreting DNA Evidence: A review. Inter. Statistical Review. 2003 [acceso: 12/06/2016].71(3):473-95.Disponible en: https://www.researchgate.net/publication/29654646
National Institute of Standards and Technology, USA. Short Tandem Repeats DNA internet Database (STRBase).2019 [acceso: 02/05/2016]. Disponible en: https://strbase.nist.gov/.
Morling N, Allen RW, Carracedo A, Geada H, Guidet F, Hallember C et al. Paternity Testing Commission of the International Society of Forensic Genetics: recommendations on genetic investigations in paternity case. Forensic Sci Inter. 2002;129:148–57.
Shriver, MD, Jin L, Chakraborty R, Boerwinkle E. VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach. Genetics.1993;134:983-93.
Fimmers R, Henke L, Henke J, Baur M. How to deal with mutations in DNA-testing, En: C. Rittner, P.M. Schneider (Eds.), Advances in Forensic Haemogenetics, vol. 4, Berlin, Springer-Verlag, Berlin, 1992:285–7.
Bär W, Brinkmann B, Budowle A, Carracedo A, Gill P, Lincoln P et al. DNA recommendations. Further report of the DNA Commission of the ISFG regarding the use of short tandem repeat systems, Forensic Sci Inter. 1997;87(3):181-4.
Gjertson DW, Brenner CH, Baur MP, Carracedo A, Guidet F, Luque JA et al. ISFG: Recommendations on biostatistics in paternity testing. Forensic Sci Inter: Genetics. 2007;1:223-31.
Schneider, PM. Scientific standards for studies in forensic genetics. Forensic Sci. Int. 2007;165:238–43.
Gill P, Gusmão L, Haned H, Mayr WR, Morling N, Parson W et al. DNA Commission of the International Society of Forensic Genetics: Recommendations on the evaluation of STR typing results that may include drop-out and/or drop-in using probabilistic methods. Forensic Sci Inter: Genetics. 2012;6(6):679-88.
Walsh PS, Metzger DA, Higuchi R. Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. BioTechniques. 1991;10:506.
Promega Corporation. Supplementary Table 2. Allele frequency values for unrelated Hispanic U.S. population at 29 autosomal STR loci. [acceso: 12/11/2019] En: https://worldwide.promega.com/Products/pm/Genetic%20Identity/Population%20Statistics/Allele%20Frequencies/?fq=allele%20frequency%20STR.
García Aceves ME, Martínez Cortés G, Rangel Villalobos H. Results obtained in five years in a paternity testing laboratory in Mexico. Forensic Sci Inter: Genetics Supplement Series. 2017;6:e305–7.
García-Aceves ME, Romero Rentería O, Díaz-Navarro XX y Rangel Villalobos H. Paternity tests in Mexico: Results obtained in 3005 cases. J. Forensic and Legal Med.2018;55:1–7
Zhang MX, Gao HM, Han SY, Liu YL. Risk analysis of duo parentage testing with limited STR loci. Genetics and Mol. Res. 2014;13(1):1179-86.
Butler JM. Genetics and Genomics of Core Short Tandem Repeat Loci Used in Human Identity Testing. J Forensic Sci. 2006 [acceso: 12/02/2009],51(2):253. Disponible en: www.blackwell-synergy.com
Coleman H, Swenson E. DNA in the Courtroom: A Trial Watcher's Guide. First ed. Seattle: Genelux Press; 1994.
Sociedad Americana de Bancos de Sangre. Annual Report Summary for Testing in 2013.[acceso: 15/06/2018] Disponible en: https://www.aabb.org/sa/facilities/Pages/relationshipreports.aspx
Bellis MA, Hughes K, Hughes S, Ashton JR. Measuring paternal discrepancy and its public health consequences. J Epid Comm Health. 2005;59:749–54.
Wolf M, Musch J, Enczmann J, Fischer J. Estimating the prevalence of non paternity in Germany. Hum Nat. 2012;23:208–17.