Butenhoff, Karin

Dolf, Gaudenz

Drögemüller, Michaela

Jagannathan, Vidhya

Kottmann-Berger, Suzanne

Leeb, Tosso

Wess, Gerhard

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1 3Hum Genet (2015) 134:127–129DOI 10.1007/s00439-014-1506-5LETTER TO THE EDITORA single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogsMichaela Drögemüller · Vidhya Jagannathan · Gaudenz Dolf · Karin Butenhoff · Suzanne Kottmann‑Berger · Gerhard Wess · Tosso Leeb Received: 10 October 2014 / Accepted: 28 October 2014 / Published online: 13 November 2014 © Springer-Verlag Berlin Heidelberg 2014define the assumed mode of inheritance, but describe a single family of 45 dogs, which supports previous older reports of a possible dominant pattern of inheritance with variable penetrance. However, Stern et al. do not cite or discuss a published study that investigated the mode of inheritance in a large dataset of more than 200,000 New-foundland dogs (Reist-Marti et al. 2012).Stern et al. further report the results from a GWAS using 18 cases and 20 control dogs, which is arguably even in purebred dogs below the required cohort size to reliably detect significant associations for traits other than fully penetrant Mendelian characters. Stern et al. did not correct for the substantial population stratification in their samples and therefore report highly inflated p values, which might represent false positive signals. Stern et al. concede in their discussion that “a single region of interest was not read-ily identified by genome-wide association study” and their GWAS did not provide any meaningful positional informa-tion on a hypothetical SAS locus.In an independent and complementary approach, Stern et al. performed an RNA-seq experiment on subvalvular ridge tissue samples from two SAS-affected Newfoundland dogs and six other non-Newfoundland dogs without SAS. They then filtered for non-synonymous variants that were exclusively present in one or both SAS-affected Newfound-land dogs and identified the PICALM:p.K599_L600insL variant. This approach is not sufficient to claim a causal relationship between this variant and SAS as it should also detect many breed-specific variants. The authors do not give any descriptive statistics as to how many reads were analyzed, how many variants were detected in total, and how many variants were exclusively found in Newfound-land dogs. If the PICALM variant was the only private non-synonymous variant found in Newfoundland dogs, then one has to conclude that the RNA-seq experiment has In their original investigation Stern et al. reported an asso-ciation of a single codon insertion in the PICALM gene (p.K599_L600insL) with familial subvalvular aortic ste-nosis (SAS) in Newfoundland dogs (Stern et al. 2014). The reported findings are the basis of a commercially sold genetic test intended to help dog breeders to reduce SAS disease prevalence. In this report, we will outline that the original investigation by Stern et al. is not well designed, misinterprets data, and consequently makes incorrect claims. Additionally, we report data from a replication study that does not show any association between the PICALM variant and SAS.In our opinion, the experimental data reported by Stern et al. do not support the conclusion of an association of the PICALM insertion with SAS. Stern et al. do not precisely This comment refers to the article available at doi:10.1007/s00439-014-1454-0.Electronic supplementary material The online version of this article (doi:10.1007/s00439-014-1506-5) contains supplementary material, which is available to authorized users.M. Drögemüller · V. Jagannathan · G. Dolf · T. Leeb (*) Vetsuisse Faculty, Institute of Genetics, University of Bern, Bremgartenstrasse 109a, 3001 Bern, Switzerlande-mail: tosso.leeb@vetsuisse.unibe.chK. Butenhoff The Newfoundlanddog Database, An der Tränke 1, 34379 Calden-Westuffeln, GermanyS. Kottmann-Berger Swiss Newfoundland Club (SNK), Schongauerstr. 3, 5618 Bettwil, SwitzerlandG. Wess Clinic of Small Animal Medicine, LMU University, 80539 Munich, Germany128 Hum Genet (2015) 134:127–1291 3technically failed. If there were other private non-synony-mous variants in the SAS-affected Newfoundland dogs, Stern et al. did not report them.Stern et al. then performed an association analysis of the PICALM variant in 26 SAS-affected Newfoundland dogs and 23 Newfoundland controls. It is not described whether these dogs were partially overlapping with the cohort used for the GWAS or with the family used for the pedigree analysis. Stern et al. found a significant association of the insertion allele with SAS (“p < 0.0001”). Stern et al. also reported that they found the insertion in three SAS-affected dogs from other breeds, but not in 180 control dogs from different breeds.Stern et al. further performed in situ histochemistry to demonstrate PICALM protein expression in cardiac tissues of two SAS-affected Newfoundland dogs that were either heterozygous or homozygous for the insertion. The pre-sented figure does not provide a control that would allow to assess the specificity of the used antibody, but even more important, there are no data from the heart of a normal con-trol dog being homozygous wildtype at the PICALM variant.Finally, Stern et al. treated developing Xenopus embryos with a small molecule inhibitor of clathrin-mediated endo-cytosis and found changes in the heart outflow tract. This is arguably a very indirect experiment. The experiment does not prove that the single codon insertion has any func-tional effect on the PICALM protein and it does not prove whether this effect indeed leads to an inhibition of clath-rin-mediated endocytosis, which is comparable to the one claimed to be caused by the used inhibitor. Therefore, the Xenopus experiment does not prove that the PICALM:p.K599_L600insL variant is causally involved in the devel-opment of SAS.As the argumentation by Stern et al. for the claimed role of the PICALM variant in SAS did not convince us, we performed a replication study in an independent cohort of dogs. We used samples from 399 Newfoundland dogs, of which 102 had been examined by specialized veterinary cardiologists during the routine screening program of the German and Swiss Newfoundland clubs. We grouped the Newfoundland dogs into five different phenotype classes: (A) dogs with unknown phenotype (n = 286); (B) dogs that were found to be SAS non-affected by a veterinarian, based upon negative auscultation findings (without a murmur), but without a documented measurement of maximal aortic outflow tract velocity (LVOT Vmax; n = 11); (C) dogs clas-sified as SAS non-affected with an LVOT Vmax <1.9 m/s (n = 88); (D) dogs classified as SAS equivocal with an LVOT Vmax = 1.9–2.4 m/s (n = 8) and (E) dogs classi-fied as SAS affected with an LVOT Vmax >2.4 m/s (n = 6). The classes C, D and E were formed with the same cri-teria as used in the study by Stern et al. We additionally used samples from 500 dogs of 64 diverse other breeds without detailed information on their SAS phenotypes. Samples from these dogs were submitted to our research laboratory in the course of other research projects and we assumed them to be free of SAS. We designed PCR prim-ers and amplified and sequenced the region containing the PICALM:p.K599_L600insL variant from all 899 dogs.The PICALM insertion had an allele frequency of 0.39 in our cohort of 399 Newfoundland dogs and it occurred in either heterozygous or homozygous state in 259 (65 %) of our Newfoundland dogs. Stern et al. state a dominant mode of action with a penetrance of 80.6 % for this allele. This means that 209 dogs or 52 % of our cohort would have been expected to be affected by SAS. In contrast to these estima-tions we were aware of only 14 either SAS-affected or SAS equivocal dogs, which represent less than 14 % of the 102 dogs in our cohort that underwent a cardiac exam. The SAS prevalence in the general Newfoundland population has Table 1  PICALM:p.K599_L600insL allele and genotype distribution in Newfoundland dogsWhile Stern et al. reported a significant association of the insertion with SAS in their cohort, there is no statistically significant difference between the allele or genotype distribution in any of the five phenotype classes investigated in this study (pallelic = 0.91; pgenotypic = 0.80; Fisher’s exact test)References Phenotype class n Allele distribution Genotype distributionwt ins wt/wt wt/ins ins/insStern et al. (2014)SAS non-affected 23 39 (0.85) 7 (0.15) 17 (0.74) 5 (0.22) 1 (0.04)SAS affected 26 18 (0.35) 34 (0.65) 1 (0.04) 16 (0.62) 9 (0.35)This studyPhenotype unknown 286 344 (0.60) 228 (0.40) 98 (0.34) 148 (0.52) 40 (0.14)SAS non-affected, LVOT Vmax unknown 11 15 (0.68) 7 (0.32) 6 (0.55) 3 (0.27) 2 (0.18)SAS non-affected, LVOT Vmax <1.9 m/s 88 106 (0.60) 70 (0.40) 30 (0.34) 46 (0.52) 12 (0.14)SAS equivocal, LVOT Vmax = 1.9–2.4 m/s 8 11 (0.69) 5 (0.31) 4 (0.50) 3 (0.38) 1 (0.13)SAS affected, LVOT Vmax >2.4 m/s 6 8 (0.67) 4 (0.33) 2 (0.33) 4 (0.67) 0 (0.00)129Hum Genet (2015) 134:127–129 1 3been reported to be less than 5 % based on more than 6,000 analyzed dogs (Reist-Marti et al. 2012).In our replication study, we neither found an allelic nor a genotypic association for the PICALM:p.K599_L600insL variant with the SAS phenotype (Table 1). Finally, we observed the insertion allele also in other breeds. In a cohort of 500 dogs from 64 breeds, 25 dogs were heterozy-gous for this variant (Table S1).In conclusion, our data strongly suggest that the PICALM:p.K599_L600insL variant is not causally involved in the development of SAS in Newfoundland dogs, but rather a neutral variant that occurs at high fre-quencies in Newfoundland dogs and is rare or absent in most other dog breeds. Consequently, the genotype at this variant is not a meaningful predictor of SAS risk. Rather, use of the commercially available genetic test has the potential to cause great harm as 65 % of the Newfoundland breed would be considered at risk for SAS and the sudden exclusion of such a large proportion of the breeding popu-lation would have a severe impact on the genetic diversity of the breed and potentially detrimental consequences regarding other (recessive) genetic defects.Acknowledgments We gratefully acknowledge the tremendous support of our research by dog owners and veterinarians who donated blood samples as well as pedigree and phenotype data. We thank Michael Deinert for helpful discussions.Conflict of interest The authors are scientific competitors of the investigators of the original study. The authors have no financial con-flict of interest to declare.ReferencesReist-Marti SB, Dolf G, Leeb T, Kottmann S, Kietzmann S, Buten-hoff K, Rieder S (2012) Genetic evidence of subaortic stenosis in the Newfoundland dog. Vet Rec 170:597. doi:10.1136/vr.100019Stern JA, White SN, Lehmkuhl LB, Reina-Doreste Y, Ferguson JL, Nascone-Yoder NM, Meurs KM (2014) A single codon insertion in PICALM is associated with development of familial subvalvu-lar aortic stenosis in Newfoundland dogs. Hum Genet 133:1139–1148. doi:10.1007/s00439-014-1454-0

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A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs

A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs

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