Diverse somatic genomic alterations in single neurons in chronic traumatic encephalopathy
Guanlan DongiD, Chanthia C. MaiD, Shulin MaoiD, Katherine Sun-Mi BrowniD, Samuel M. NaikiD, Gannon A. McDonoughiD, Samadhi P. Wijethunga, Junho KimiD, Samantha L. KirkhamiD, Diane D. ShaoiD, Jonathan D. CherryiD, Madeline UretskyiD, Elizabeth SpurlockiD, Ann Carolyn McKeeiD, August Yue HuangiD, Michael B. MilleriD, Eunjung Alice LeeiD, Christopher A. WalshiD
Abstract
Chronic traumatic encephalopathy (CTE) is a neurodegenerative disease that is linked to exposure to repetitive head impacts (RHI), yet little is known about its pathogenesis. Applying two single-cell whole-genome sequencing methods to hundreds of neurons from prefrontal cortex of 15 individuals with CTE, and 4 with RHI without CTE, revealed increased somatic single-nucleotide variants in CTE, resembling a pattern previously reported in Alzheimers disease (AD). Furthermore, we discovered remarkably high burdens of somatic small insertions and deletions in a subset of CTE individuals, resembling a known pattern, ID4, also found in AD. Our results suggest that neurons in CTE experience stereotyped mutational processes shared with AD; the absence of similar changes in RHI neurons without CTE suggests that CTE involves mechanisms beyond RHI alone.
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