Alzheimer Disease Pathology-Associated Polymorphism in a Complex Variable Number of Tandem Repeat Region Within the MUC6 Gene, Near the AP2A2 Gene. Issue 1 (4th November 2019)

• Record Type: Journal Article
• Authors: Katsumata, Yuriko; Fardo, David W; Bachstetter, Adam D; Artiushin, Sergey C; Wang, Wang-Xia; Wei, Angela; Brzezinski, Lena J; Nelson, Bela G; Huang, Qingwei; Abner, Erin L; Anderson, Sonya; Patel, Indumati; Shaw, Benjamin C; Price, Douglas A; Niedowicz, Dana M; Wilcock, Donna W; Jicha, Gregory A; Neltner, Janna H; Van Eldik, Linda J; Estus, Steven; Nelson, Peter T
• Is Part Of: Journal of neuropathology and experimental neurology. Volume 79:Issue 1(2020)
• Page Start: 3
• Page End: 21
• Publication Date: 2019-11-04
• Subjects: ADSP -- AP-2 -- Digital pathology -- GWAS -- ScanScope -- Whole-exome sequencing; Neurology -- Diseases -- Periodicals; Neurology -- Diseases -- Physiopathology -- Periodicals; 616.8047
• DOI: 10.1093/jnen/nlz116
• Languages: English
• ISSNs: 0022-3069

Abstract

Abstract: We found evidence of late-onset Alzheimer disease (LOAD)-associated genetic polymorphism within an exon of Mucin 6 ( MUC6) and immediately downstream from another gene: Adaptor Related Protein Complex 2 Subunit Alpha 2 ( AP2A2 ). PCR analyses on genomic DNA samples confirmed that the size of the MUC6 variable number tandem repeat ( VNTR) region was highly polymorphic. In a cohort of autopsied subjects with quantitative digital pathology data (n = 119), the size of the polymorphic region was associated with the severity of pTau pathology in neocortex. In a separate replication cohort of autopsied subjects (n = 173), more pTau pathology was again observed in subjects with longer VNTR regions (p = 0.031). Unlike MUC6, AP2A2 is highly expressed in human brain. AP2A2 expression was lower in a subset analysis of brain samples from persons with longer versus shorter VNTR regions (p = 0.014 normalizing with AP2B1 expression). Double-label immunofluorescence studies showed that AP2A2 protein often colocalized with neurofibrillary tangles in LOAD but was not colocalized with pTau proteinopathy in progressive supranuclear palsy, or with TDP-43 proteinopathy. In summary, polymorphism in a repeat-rich region near AP2A2 was associated with neocortical pTau proteinopathy (because of the unique repeats, prior genome-wide association studies were probably unable to detect this association), and AP2A2 was often colocalized with neurofibrillary tangles in LOAD.