Department of Biomedicine, Aarhus University, Høegh-Guldbergs Gade 10, 8000, Aarhus C, Denmark.
Department of Neuroscience, Mayo Clinic, Jacksonville, FL, 32224, USA.
Acta Neuropathol Commun. 2021 Mar 16;9(1):43. doi: 10.1186/s40478-021-01140-7.
SORL1 is strongly associated with both sporadic and familial forms of Alzheimer's disease (AD), but a lack of information about alternatively spliced transcripts currently limits our understanding of the role of SORL1 in AD. Here, we describe a SORL1 transcript (SORL1-38b) characterized by inclusion of a novel exon (E38b) that encodes a truncated protein. We identified E38b-containing transcripts in several brain regions, with the highest expression in the cerebellum and showed that SORL1-38b is largely located in neuronal dendrites, which is in contrast to the somatic distribution of transcripts encoding the full-length SORLA protein (SORL1-fl). SORL1-38b transcript levels were significantly reduced in AD cerebellum in three independent cohorts of postmortem brains, whereas no changes were observed for SORL1-fl. A trend of lower 38b transcript level in cerebellum was found for individuals carrying the risk variant at rs2282649 (known as SNP24), although not reaching statistical significance. These findings suggest synaptic functions for SORL1-38b in the brain, uncovering novel aspects of SORL1 that can be further explored in AD research.
SORL1 与散发性和家族性阿尔茨海默病(AD)密切相关,但目前对选择性剪接转录本的了解有限,限制了我们对 SORL1 在 AD 中的作用的理解。在这里,我们描述了一种 SORL1 转录本(SORL1-38b),其特征是包含一个新的外显子(E38b),该外显子编码一个截断的蛋白质。我们在几个大脑区域中鉴定出含有 E38b 的转录本,在小脑中的表达最高,并表明 SORL1-38b 主要位于神经元树突中,这与编码全长 SORLA 蛋白(SORL1-fl)的转录本的体细胞分布形成对比。在三个独立的尸检大脑队列中,AD 小脑中的 SORL1-38b 转录本水平显著降低,而 SORL1-fl 没有变化。尽管没有达到统计学意义,但在携带 rs2282649 风险变异体(称为 SNP24)的个体中,小脑中 38b 转录本水平较低的趋势。这些发现表明 SORL1-38b 在大脑中的突触功能,揭示了 SORL1 的新方面,可以在 AD 研究中进一步探索。