[1] |
Wang B, Yang W, Wen W, et al. Gamma⁃secretase gene mutations in familial acne inversa[J]. Science, 2010,330(6007):1065. doi: 10.1126/science.1196284.
|
[2] |
McMillan BJ, Zimmerman B, Egan ED, et al. Structure of human POFUT1, its requirement in ligand⁃independent oncogenic Notch signaling, and functional effects of Dowling⁃Degos mutations[J]. Glycobiology, 2017,27(8):777⁃786. doi: 10.1093/glycob/cwx020.
|
[3] |
Zhou C, Wen GD, Soe LM, et al. Novel mutations in PSENEN gene in two Chinese acne inversa families manifested as familial multiple comedones and Dowling⁃Degos disease[J]. Chin Med J (Engl), 2016,129(23):2834⁃2839. doi: 10.4103/0366⁃6999.19 4648.
|
[4] |
Pavlovsky M, Sarig O, Eskin⁃Schwartz M, et al. A phenotype combining hidradenitis suppurativa with Dowling⁃Degos disease caused by a founder mutation in PSENEN[J]. Br J Dermatol, 2018,178(2):502⁃508. doi: 10.1111/bjd.16000.
|
[5] |
Ralser DJ, Basmanav FB, Tafazzoli A, et al. Mutations in γ⁃secretase subunit⁃encoding PSENEN underlie Dowling⁃Degos disease associated with acne inversa[J]. J Clin Invest, 2017,127(4):1485⁃1490. doi: 10.1172/JCI90667.
|
[6] |
Hsu CH, Liou GG, Jiang YJ. Nicastrin deficiency induces tyrosinase⁃dependent depigmentation and skin inflammation[J]. J Invest Dermatol, 2020,140(2):404⁃414. doi: 10.1016/j.jid.2019. 07.702.
|
[7] |
Garcovich S, Tricarico PM, Nait⁃Meddour C, et al. Novel nicastrin mutation in hidradenitis suppurativa⁃Dowling⁃Degos disease clinical phenotype: more than just clinical overlap?[J]. Br J Dermatol, 2020,183(4):758⁃759. doi: 10.1111/bjd.19121.
|
[8] |
Bai XC, Yan C, Yang G, et al. An atomic structure of human γ⁃secretase[J]. Nature, 2015,525(7568):212⁃217. doi: 10.1038/nature14892.
|
[9] |
Li Y, Liew LS, Li Q, et al. Structure of the transmembrane domain of human nicastrin⁃a component of γ⁃secretase[J]. Sci Rep, 2016,6:19522.
|
[10] |
Bolduc DM, Montagna DR, Gu Y, et al. Nicastrin functions to sterically hinder γ⁃secretase⁃substrate interactions driven by substrate transmembrane domain[J]. Proc Natl Acad Sci U S A, 2016,113(5):E509⁃ E518. doi: 10.1073/pnas.1512952113.
|
[11] |
Güner G, Lichtenthaler SF. The substrate repertoire of γ⁃secretase/presenilin[J]. Semin Cell Dev Biol, 2020,105:27⁃42. doi: 10.1016/j.semcdb.2020.05.019.
|
[12] |
Wang R, Tang P, Wang P, et al. Regulation of tyrosinase trafficking and processing by presenilins: partial loss of function by familial Alzheimer′s disease mutation[J]. Proc Natl Acad Sci U S A, 2006,103(2):353⁃358. doi: 10.1073/pnas.0509822102.
|
[13] |
Zanotti S, Canalis E. Notch signaling and the skeleton[J]. Endocr Rev, 2016,37(3):223⁃253. doi: 10.1210/er.2016⁃1002.
|
[14] |
Xiao X, He Y, Li C, et al. Nicastrin mutations in familial acne inversa impact keratinocyte proliferation and differentiation through the Notch and phosphoinositide 3⁃kinase/AKT signalling pathways[J]. Br J Dermatol, 2016,174(3):522⁃532. doi: 10.1111/bjd.14223.
|
[15] |
Li C, Li W, Xu H, et al. PSENEN mutation carriers with co⁃manifestation of acne inversa (AI) and Dowling⁃Degos disease (DDD): is AI or DDD the subphenotype?[J]. J Invest Dermatol, 2017,137(10):2234⁃2236. doi: 10.1016/j.jid.2017.05.021.
|
[16] |
Strub T, Giuliano S, Ye T, et al. Essential role of microphthalmia transcription factor for DNA replication, mitosis and genomic stability in melanoma[J]. Oncogene, 2011,30(20):2319⁃2332. doi: 10.1038/onc.2010.612.
|
[17] |
Ernfors P. Cellular origin and developmental mechanisms during the formation of skin melanocytes[J]. Exp Cell Res, 2010,316(8):1397⁃1407. doi: 10.1016/j.yexcr.2010.02.042.
|
[18] |
Nguyen NT, Fisher DE. MITF and UV responses in skin: from pigmentation to addiction[J]. Pigment Cell Melanoma Res, 2019,32(2):224⁃236. doi: 10.1111/pcmr.12726.
|
[19] |
Mort RL, Jackson IJ, Patton EE. The melanocyte lineage in development and disease[J]. Development, 2015,142(4):620⁃632. doi: 10.1242/dev.106567.
|
[20] |
Watt B, van Niel G, Raposo G, et al. PMEL: a pigment cell⁃specific model for functional amyloid formation[J]. Pigment Cell Melanoma Res, 2013,26(3):300⁃315. doi: 10.1111/pcmr.12067.
|
[21] |
Kummer MP, Maruyama H, Huelsmann C, et al. Formation of Pmel17 amyloid is regulated by juxtamembrane metalloproteinase cleavage, and the resulting C⁃terminal fragment is a substrate for gamma⁃secretase[J]. J Biol Chem, 2009,284(4):2296⁃2306. doi: 10.1074/jbc.M808904200.
|