Genome-wide association study and functional validation implicates JADE1 in tauopathy

被引:20
作者
Farrell, Kurt [1 ,2 ,3 ]
Kim, SoongHo [1 ,2 ,3 ]
Han, Natalia [1 ,2 ,3 ]
Iida, Megan A. [1 ,2 ,3 ]
Gonzalez, Elias M. [4 ]
Otero-Garcia, Marcos [5 ]
Walker, Jamie M. [6 ,7 ]
Richardson, Timothy E. [6 ,7 ]
Renton, Alan E. [2 ,8 ]
Andrews, Shea J. [2 ,8 ]
Fulton-Howard, Brian [2 ,8 ]
Humphrey, Jack [2 ,8 ]
Vialle, Ricardo A. [2 ,8 ]
Bowles, Kathryn R. [8 ]
Lopes, Katia de Paiva [2 ,8 ]
Whitney, Kristen [1 ,2 ,3 ]
Dangoor, Diana K. [1 ,2 ,3 ]
Walsh, Hadley [1 ,2 ,3 ]
Marcora, Edoardo [2 ,8 ]
Hefti, Marco M. [9 ]
Casella, Alicia [1 ,2 ,3 ]
Sissoko, Cheick T. [1 ,2 ,3 ]
Kapoor, Manav [2 ,8 ]
Novikova, Gloriia [2 ,8 ]
Udine, Evan [2 ,8 ]
Wong, Garrett [2 ,8 ]
Tang, Weijing [38 ]
Bhangale, Tushar [10 ]
Hunkapiller, Julie [10 ]
Ayalon, Gai [11 ]
Graham, Robert R. [12 ]
Cherry, Jonathan D. [13 ]
Cortes, Etty P. [1 ,2 ]
Borukov, Valeriy Y. [1 ,2 ]
McKee, Ann C. [13 ]
Stein, Thor D. [13 ]
Vonsattel, Jean-Paul [14 ,15 ,16 ]
Teich, Andy F. [14 ,15 ,16 ]
Gearing, Marla [17 ]
Glass, Jonathan [17 ]
Troncoso, Juan C. [18 ]
Frosch, Matthew P. [19 ,20 ]
Hyman, Bradley T. [19 ,20 ]
Dickson, Dennis W. [21 ]
Murray, Melissa E. [21 ]
Attems, Johannes [22 ]
Flanagan, Margaret E. [23 ]
Mao, Qinwen [23 ]
Mesulam, M-Marsel [23 ]
Weintraub, Sandra [23 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Pathol, Neuropathol Brain Bank & Res CoRE, 1 Gustave L Levy Pl Box 1194, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Nash Dept Neurosci, Ronald M Loeb Ctr Alzheimers Dis, Friedman Brain Inst, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Artificial Intelligence & Human Hlth, New York, NY 10029 USA
[4] Univ Texas Hlth San Antonio, Dept Cell Syst & Anat, Glenn Biggs Inst Alzheimers & Neurodegenerat Dis, Sam & Ann Barshop Inst Longev & Aging Studies, San Antonio, TX 78229 USA
[5] Univ Calif Los Angeles, Div Neuropathol, Dept Pathol & Lab Med, Los Angeles, CA USA
[6] UT Hlth San Antonio, Dept Pathol, San Antonio, TX USA
[7] UT Hlth San Antonio, Glenn Biggs Inst Alzheimers & Neurodegenerat Dis, San Antonio, TX USA
[8] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[9] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
[10] Genentech Inc, Dept Human Genet, San Francisco, CA 94080 USA
[11] Neumora Therapeut, San Francisco, CA USA
[12] Maze Therapeut, San Francisco, CA USA
[13] Boston Univ, Sch Med, Dept Pathol Neuropathol, VA Med Ctr, Boston, MA 02118 USA
[14] Columbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY USA
[15] Columbia Univ, Med Ctr, Dept Neurol, New York, NY USA
[16] Columbia Univ, Med Ctr, Taub Inst Res Alzheimers Dis & Aging Brain, New York, NY USA
[17] Emory Univ, Sch Med, Dept Pathol & Lab Med Neuropathol & Neurol, Atlanta, GA USA
[18] Johns Hopkins Univ, Sch Med, Dept Pathol, Div Neuropathol, Baltimore, MD 21205 USA
[19] Harvard Med Sch, Dept Neurol & Pathol, Charlestown, MA USA
[20] Massachusetts Gen Hosp, Charlestown, MA USA
[21] Mayo Clin, Dept Neurosci, Jacksonville, FL USA
[22] Newcastle Univ, Translat & Clin Res Inst, Newcastle Upon Tyne, Tyne & Wear, England
[23] Northwestern Univ, Dept Pathol Neuropathol, Northwestern Cognit Neurol & Alzheimer Dis Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
[24] Oregon Hlth & Sci Univ, Dept Pathol, Portland, OR USA
[25] Univ Pittsburgh, Dept Pathol Neuropathol, Med Ctr, Pittsburgh, PA USA
[26] Rush Univ, Med Ctr, Dept Pathol Neuropathol, Chicago, IL USA
[27] Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL USA
[28] Icahn Sch Med Mt Sinai, Dept Psychiat, Alzheimers Dis Res Ctr, James J Peters VA Med Ctr, New York, NY 10029 USA
[29] Banner Sun Hlth Res Inst, Dept Neuropathol, Sun City, AZ USA
[30] UC Irvine, Dept Neurol, Dept Epidemiol, Inst Memory Impairments & Neurol Disorders, Irvine, CA USA
[31] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[32] Vet Affairs San Diego Healthcare Syst, San Diego, CA USA
[33] Univ Kentucky, Dept Pathol Neuropathol, Lexington, KY USA
[34] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
[35] Univ Penn, Dept Pathol & Lab Med, Ctr Neurodegenerat Dis Res, Perelman Sch Med, Philadelphia, PA USA
[36] Univ Penn, Dept Neurol, Perelman Sch Med, Philadelphia, PA 19104 USA
[37] Univ Washington, Dept Lab Med & Pathol, Sch Med, Seattle, WA USA
[38] Stanford Univ, Dept Pathol, Palo Alto, CA 94304 USA
[39] Univ Hlth Network, Krembil Brain Inst, Lab Med Program, Toronto, ON, Canada
[40] Univ Toronto, Tanz Ctr Res Neurodegenerat Dis, Toronto, ON, Canada
[41] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[42] Med Univ Vienna, Inst Neurol, Vienna, Austria
[43] Washington Univ, Sch Med, Dept Pathol & Immunol, Dept Neurol,Knight Alzheimer Dis Res Ctr, St Louis, MO USA
[44] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA
[45] Boston Univ, Sch Med, Dept Pathol, Boston, MA 02118 USA
[46] Boston Univ, Sch Med, Dept Pharmacol, Boston, MA 02118 USA
[47] Boston Med Ctr, Boston, MA USA
[48] Univ Texas Southwestern Med Sch Dallas, Dept Pathol Neuropathol, Dallas, TX USA
[49] Univ Exeter, Coll Med & Hlth, Exeter, Devon, England
[50] Icahn Sch Med Mt Sinai, Ctr Cognit Hlth, Dept Neurol, New York, NY 10029 USA
基金
英国医学研究理事会;
关键词
PROGRESSIVE SUPRANUCLEAR PALSY; AGE-RELATED TAUOPATHY; CRYO-EM STRUCTURES; TUMOR-SUPPRESSOR; NEUROFIBRILLARY TANGLES; SENILE-DEMENTIA; RISK LOCI; COGNITIVE IMPAIRMENT; TAU PATHOLOGY; OLDER PERSONS;
D O I
10.1007/s00401-021-02379-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Primary age-related tauopathy (PART) is a neurodegenerative pathology with features distinct from but also overlapping with Alzheimer disease (AD). While both exhibit Alzheimer-type temporal lobe neurofibrillary degeneration alongside amnestic cognitive impairment, PART develops independently of amyloid-beta (A beta) plaques. The pathogenesis of PART is not known, but evidence suggests an association with genes that promote tau pathology and others that protect from A beta toxicity. Here, we performed a genetic association study in an autopsy cohort of individuals with PART (n = 647) using Braak neurofibrillary tangle stage as a quantitative trait. We found some significant associations with candidate loci associated with AD (SLC24A4, MS4A6A, HS3ST1) and progressive supranuclear palsy (MAPT and EIF2AK3). Genome-wide association analysis revealed a novel significant association with a single nucleotide polymorphism on chromosome 4 (rs56405341) in a locus containing three genes, including JADE1 which was significantly upregulated in tangle-bearing neurons by single-soma RNA-seq. Immunohistochemical studies using antisera targeting JADE1 protein revealed localization within tau aggregates in autopsy brains with four microtubule-binding domain repeats (4R) isoforms and mixed 3R/4R, but not with 3R exclusively. Co-immunoprecipitation in post-mortem human PART brain tissue revealed a specific binding of JADE1 protein to four repeat tau lacking N-terminal inserts (0N4R). Finally, knockdown of the Drosophila JADE1 homolog rhinoceros (rno) enhanced tau-induced toxicity and apoptosis in vivo in a humanized 0N4R mutant tau knock-in model, as quantified by rough eye phenotype and terminal deoxynucleotidyl transferase dUTP nick end-labeling (TUNEL) in the fly brain. Together, these findings indicate that PART has a genetic architecture that partially overlaps with AD and other tauopathies and suggests a novel role for JADE1 as a modifier of neurofibrillary degeneration.
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收藏
页码:33 / 53
页数:21
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