SDR9C7 missense variant in a Chihuahua with non-epidermolytic ichthyosis

被引:4
作者
Kiener, Sarah [1 ,2 ]
Castilla, Eloy [3 ]
Jagannathan, Vidhya [1 ,2 ]
Welle, Monika [2 ,4 ]
Leeb, Tosso [1 ,2 ,5 ]
机构
[1] Univ Bern, Inst Genet, Vetsuisse Fac, Bern, Switzerland
[2] Univ Bern, DermFocus, Bern, Switzerland
[3] VetLutry SA, SwissVetGrp, Lutry, Switzerland
[4] Univ Bern, Inst Anim Pathol, Vetsuisse Fac, Bern, Switzerland
[5] Univ Bern, Inst Genet, Vetsuisse Fac, CH-3001 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
animal model; Canis lupus familiaris; dermatology; dog; genodermatosis; precision medicine; skin; veterinary medicine; RECESSIVE CONGENITAL ICHTHYOSIS; MUTATIONS;
D O I
10.1111/age.13319
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Ichthyoses represent a heterogeneous group of cornification disorders that are associated with skin barrier defects. We investigated a 9-month-old Chihuahua showing excessive scale formation. Clinical and histopathological examinations revealed non-epidermolytic ichthyosis and a genetic defect was suspected. We therefore sequenced the genome of the affected dog and compared the data with 564 genetically diverse control genomes. Filtering for private variants identified a homozygous missense variant in SDR9C7, c.454C>T or p.(Arg152Trp). SDR9C7 is a known candidate gene for ichthyosis in humans and encodes the short-chain dehydrogenase/reductase family 9C member 7. The enzyme is involved in the production of a functional corneocyte lipid envelope (CLE), a crucial component of the epidermal barrier. Pathogenic variants in SDR9C7 have been described in human patients with autosomal recessive ichthyosis. We assume that the identified missense variant in the affected Chihuahua of this study impairs the normal enzymatic activity of SDR9C7 and thus prevents the formation of a functioning CLE, resulting in a defective skin barrier. To the best of our knowledge, this is the first report of a spontaneous SDR9C7 variant in domestic animals.
引用
收藏
页码:562 / 565
页数:4
相关论文
共 24 条
[1]   An update on molecular aspects of the non-syndromic ichthyoses [J].
Akiyama, Masashi ;
Shimizu, Hiroshi .
EXPERIMENTAL DERMATOLOGY, 2008, 17 (05) :373-382
[2]   Acylceramide is a key player in skin barrier function: insight into the molecular mechanisms of skin barrier formation and ichthyosis pathogenesis [J].
Akiyama, Masashi .
FEBS JOURNAL, 2021, 288 (07) :2119-2130
[3]   Corneocyte lipid envelope (CLE), the key structure for skin barrier function and ichthyosis pathogenesis [J].
Akiyama, Masashi .
JOURNAL OF DERMATOLOGICAL SCIENCE, 2017, 88 (01) :3-9
[4]   PredictSNP: Robust and Accurate Consensus Classifier for Prediction of Disease-Related Mutations [J].
Bendl, Jaroslav ;
Stourac, Jan ;
Salanda, Ondrej ;
Pavelka, Antonin ;
Wieben, Eric D. ;
Zendulka, Jaroslav ;
Brezovsky, Jan ;
Damborsky, Jiri .
PLOS COMPUTATIONAL BIOLOGY, 2014, 10 (01)
[5]   PROVEAN web server: a tool to predict the functional effect of amino acid substitutions and indels [J].
Choi, Yongwook ;
Chan, Agnes P. .
BIOINFORMATICS, 2015, 31 (16) :2745-2747
[6]   Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid Envelope [J].
Crumrine, Debra ;
Khnykin, Denis ;
Krieg, Peter ;
Man, Mao-Qiang ;
Celli, Anna ;
Mauro, Theodora M. ;
Wakefield, Joan S. ;
Menon, Gopinathan ;
Mauldin, Elizabeth ;
Miner, Jeffrey H. ;
Lin, Meei-Hua ;
Brash, Alan R. ;
Sprecher, Eli ;
Radner, Franz P. W. ;
Choate, Keith ;
Roop, Dennis ;
Uchida, Yoshikazu ;
Gruber, Robert ;
Schmuth, Matthias ;
Elias, Peter M. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2019, 139 (04) :760-768
[7]   Formation and functions of the corneocyte lipid envelope (CLE) [J].
Elias, Peter M. ;
Gruber, Robert ;
Crumrine, Debra ;
Menon, Gopinathan ;
Williams, Mary L. ;
Wakefield, Joan S. ;
Holleran, Walter M. ;
Uchida, Yoshikazu .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2014, 1841 (03) :314-318
[8]   PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans [J].
Grall, Anais ;
Guaguere, Eric ;
Planchais, Sandrine ;
Grond, Susanne ;
Bourrat, Emmanuelle ;
Hausser, Ingrid ;
Hitte, Christophe ;
Le Gallo, Matthieu ;
Derbois, Celine ;
Kim, Gwang-Jin ;
Lagoutte, Laetitia ;
Degorce-Rubiales, Frederique ;
Radner, Franz P. W. ;
Thomas, Anne ;
Kury, Sebastien ;
Bensignor, Emmanuel ;
Fontaine, Jacques ;
Pin, Didier ;
Zimmermann, Robert ;
Zechner, Rudolf ;
Lathrop, Mark ;
Galibert, Francis ;
Andre, Catherine ;
Fischer, Judith .
NATURE GENETICS, 2012, 44 (02) :140-147
[9]   Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis [J].
Hotz, A. ;
Fagerberg, C. ;
Vahlquist, A. ;
Bygum, A. ;
Torma, H. ;
Rauschendorf, M-A ;
Zhang, H. ;
Heinz, L. ;
Bourrat, E. ;
Hausser, I. ;
Vestergaard, V. ;
Dragomir, A. ;
Zimmer, A. D. ;
Fischer, J. .
BRITISH JOURNAL OF DERMATOLOGY, 2018, 178 (03) :E207-E209
[10]   A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves [J].
Jagannathan, V ;
Droegemueller, C. ;
Leeb, T. ;
Aguirre, Gustavo ;
Andre, Catherine ;
Bannasch, Danika ;
Becker, Doreen ;
Davis, Brian ;
Drogemuller, Cord ;
Ekenstedt, Kari ;
Faller, Kiterie ;
Forman, Oliver ;
Friedenberg, Steve ;
Furrow, Eva ;
Giger, Urs ;
Hitte, Christophe ;
Hytonen, Marjo ;
Lohi, Hannes ;
Mellersh, Cathryn ;
Mickelson, James R. ;
Murgiano, Leonardo ;
Oberbauer, Anita ;
Schmutz, Sheila ;
Schoenebeck, Jeffrey ;
Summers, Kim ;
van Steenbeek, Frank ;
Wade, Claire .
ANIMAL GENETICS, 2019, 50 (06) :695-704