A general method to assess the utility of the X-chromosomal markers in kinship testing

被引:20
|
作者
Pinto, Nadia [1 ,2 ,3 ]
Silva, Pedro V. [2 ,3 ]
Amorim, Antonio [1 ,2 ]
机构
[1] Univ Porto, Inst Patol & Imunol Mol, P-4200465 Oporto, Portugal
[2] Univ Porto, Fac Ciencias, P-4200465 Oporto, Portugal
[3] Univ Porto, Ctr Matemat, P-4200465 Oporto, Portugal
关键词
Genetic evidence; Kinship testing; Identity-by-descent; X-chromosome; Genotypic probabilities; Distinguishing pedigrees; IDENTIFICATION;
D O I
10.1016/j.fsigen.2011.04.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In studies involving pedigree reconstruction and kinship estimation, it is acknowledged that some pedigrees have the same algebraic expressions for the joint genotypic probabilities and are, therefore, indistinguishable when considering only genetic information, no matter what the mode of transmission considered. Indeed, although standard forensic practice considers solely unlinked autosomal markers, the existence of pedigrees with the referred theoretical property (that are then said to belong to the same kinship class) is possible when considering any kind of genetic transmission. The research on genetic relatedness has always been linked to the root concept of identity-by-descent (IBD). However, although the basic theoretical core for autosomal transmission has been long formalised, a general method allowing the decision if two pedigrees linking two non-inbred individuals are distinguishable using unlinked autosomal markers along with the respective IBD partitions (and consequently the algebraic expressions for the joint genotypic probabilities) was only recently published. In this work X-chromosomal transmission will be at stake, considering that the analytical framework for X-chromosomal markers has been recently established and the importance of X-chromosome markers for these questions has been steadily growing, particularly in forensics, as a tool both to complement the information given by autosomes in complex kinship testing cases and to differentiate pedigrees belonging to the same autosomal kinship class. Therefore, here it will be presented a formal and mathematically well supported framework where a general counting rule is given, allowing a secure and expeditious decision on the usefulness of typing (unlinked) X-chromosomal markers on pairwise kinship testing involving two non-inbred individuals. Moreover the counting rule now presented allows the derivation of algebraic expressions for the joint genotypic probabilities associated with any pedigree. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:198 / 207
页数:10
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共 42 条
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    VANDERHORST, J
    WESTERVELD, A
    BOOTSMA, D
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    NUSSBAUM, RL
    LEWIS, RA
    LESKO, JG
    FERRELL, R
    HUMAN GENETICS, 1985, 70 (01) : 45 - 50
  • [34] REEVALUATION OF THE LINKAGE OF AN OPTIC ATROPHY SUSCEPTIBILITY GENE TO X-CHROMOSOMAL MARKERS IN FINNISH FAMILIES WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY (LHON)
    JUVONEN, V
    VILKKI, J
    AULA, P
    NIKOSKELAINEN, E
    SAVONTAUS, ML
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (01) : 289 - 292
  • [35] GENETIC-LINKAGE STUDY BETWEEN THE LOCI FOR DUCHENNE AND BECKER MUSCULAR-DYSTROPHY AND 9 X-CHROMOSOMAL DNA MARKERS
    WILICHOWSKI, E
    KRAWCZAK, M
    SEEMANOVA, E
    HANEFELD, F
    SCHMIDTKE, J
    HUMAN GENETICS, 1987, 75 (01) : 32 - 40
  • [36] Allele frequency distribution of twelve X-chromosomal short tandem repeat markers in four U.S. population groups
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  • [37] A new assay for the genetic study of general anesthesia in Drosophila melanogaster:: Use in analysis of mutations in the X-chromosomal 12E region
    Guan, ZH
    Scott, RL
    Nash, HA
    JOURNAL OF NEUROGENETICS, 2000, 14 (01) : 25 - 42
  • [38] X-chromosome markers in kinship testing: A generalisation of the IBD approach identifying situations where their contribution is crucial
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    FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2011, 5 (01) : 27 - 32
  • [39] ISOLATION, SUBCLONING AND RFLP STUDIES OF THE GENOMIC ENVIRONMENT OF THE HUMAN X-CHROMOSOMAL DNA MARKERS (DXS7), 754 (DXS84) AND C7 (DXS28)
    VANOMMEN, GJB
    BAKKER, E
    HOFKER, MH
    FISSERGROEN, Y
    BURMEISTER, M
    MANDEL, JL
    WROGEMANN, K
    PEARSON, PL
    CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 769 - 769
  • [40] ISOLATION OF DNA MARKERS FROM A REGION BETWEEN INCONTINENTIA-PIGMENTI-1 (IP1) X-CHROMOSOMAL TRANSLOCATION BREAKPOINTS BY A COMPARATIVE PCR ANALYSIS OF A RADIATION HYBRID SUBCLONE MAPPING PANEL
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