2010
DOI: 10.1007/s00251-010-0475-7
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MHC class I and MHC class II DRB gene variability in wild and captive Bengal tigers (Panthera tigris tigris)

Abstract: Bengal tigers are highly endangered and knowledge on adaptive genetic variation can be essential for efficient conservation and management. Here we present the first assessment of allelic variation in major histocompatibility complex (MHC) class I and MHC class II DRB genes for wild and captive tigers from India. We amplified, cloned, and sequenced alpha-1 and alpha-2 domain of MHC class I and beta-1 domain of MHC class II DRB genes in 16 tiger specimens of different geographic origin. We detected high variabi… Show more

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Cited by 34 publications
(38 citation statements)
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“…However, we did not find signatures of long-term positive selection in the form of an increased d N /d S ratio at ABS for any MHC family. Contrastingly, such positive selection signals were previously described in analyses of MHCI in cheetah [30], bengal tiger [32] and leopard [31], and for MHCII-DRB in eight different Felidae lineages [28], cheetah [30], but not in bengal tiger [32], leopard [31] or Eurasian lynx [29]. Interestingly, for MHCI we found d S at the ABS to be much larger than d S at non-ABS, this indicates that the ABS regions are older than non-ABS and points to positive selection acting in presence of recurrent gene conversion events [45].…”
Section: Discussionmentioning
confidence: 95%
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“…However, we did not find signatures of long-term positive selection in the form of an increased d N /d S ratio at ABS for any MHC family. Contrastingly, such positive selection signals were previously described in analyses of MHCI in cheetah [30], bengal tiger [32] and leopard [31], and for MHCII-DRB in eight different Felidae lineages [28], cheetah [30], but not in bengal tiger [32], leopard [31] or Eurasian lynx [29]. Interestingly, for MHCI we found d S at the ABS to be much larger than d S at non-ABS, this indicates that the ABS regions are older than non-ABS and points to positive selection acting in presence of recurrent gene conversion events [45].…”
Section: Discussionmentioning
confidence: 95%
“…Also the transcripts from two different Iberian lynxes annotated as MHCI or MHCII-DRB by the Iberian lynx genome project [35] were included. Primers were designed in approximately the same regions as the ones used in previous studies on MHC variation in the Felidae to enable comparisons [28, 3032]. More specifically, MHCI primers spanned bases 2 to 21 (forward) and 253 to 271 (reverse) of the human MHC class I exon 2 and MHC class II-DRB spanned bases 4 to 23 (forward) and 270 to 288 (reverse) of the human homologues [7880].…”
Section: Methodsmentioning
confidence: 99%
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“…Arguably, it is difficult to estimate “ecological meaningful” genetic diversity by solely measuring the neutral genetic diversity. In a recent review of MHC diversity and viability in natural populations, each case study included at least some populations that had undergone a decrease in population size (i.e., like our study) (Radwan et al 2010). A majority of these case studies showed a significant positive correlation between neutral markers with MHC AR, contrary to our study.…”
Section: Discussionmentioning
confidence: 99%
“…For example, a total of 10 alleles (9 functional alleles and 1 pseudo-allele) were detected from 4 putative MHC class I loci in 108 Namibian cheetahs, averaging 2.5 alleles per locus [34]. While 13 putatively functional alleles and one pseudo-allele were found from at least 4 MHC class I loci in 16 highly endangered India Bengal tigers [35]. Furthermore, Aime -MHC class II genes also showed higher polymorphism relative to other endangered species [27].…”
Section: Discussionmentioning
confidence: 99%