Patient-derived gene and protein expression signatures of NGLY1 deficiency. (8th December 2021)

• Record Type: Journal Article
• Authors: Rauscher, Benedikt; Mueller, William F; Clauder-Münster, Sandra; Jakob, Petra; Islam, M Saiful; Sun, Han; Ghidelli-Disse, Sonja; Boesche, Markus; Bantscheff, Marcus; Pflaumer, Hannah; Collier, Paul; Haase, Bettina; Chen, Songjie; Hoffman, Rene; Wang, Guangwen; Benes, Vladimir; Drewes, Gerard; Snyder, Michael; Steinmetz, Lars M
• Is Part Of: Journal of biochemistry. Volume 171:Number 2(2022)
• Page Start: 187
• Page End: 199
• Publication Date: 2021-12-08
• Subjects: NGLY1 deficiency -- patient-derived cell lines -- multi-omics profiling -- RNA sequencing -- N-glycanase 1; Biochemistry -- Periodicals; Biochemistry -- Periodicals; Electronic journals; 572.05
• DOI: 10.1093/jb/mvab131
• Languages: English
• ISSNs: 0021-924X

Abstract

Abstract: N-Glycanase 1 (NGLY1) deficiency is a rare and complex genetic disorder. Although recent studies have shed light on the molecular underpinnings of NGLY1 deficiency, a systematic characterization of gene and protein expression changes in patient-derived cells has been lacking. Here, we performed RNA-sequencing and mass spectrometry to determine the transcriptomes and proteomes of 66 cell lines representing four different cell types derived from 14 NGLY1 deficient patients and 17 controls. Although NGLY1 protein levels were up to 9.5-fold downregulated in patients compared with parents, residual and likely non-functional NGLY1 protein was detectable in all patient-derived lymphoblastoid cell lines. Consistent with the role of NGLY1 as a regulator of the transcription factor Nrf1, we observed a cell type-independent downregulation of proteasomal genes in NGLY1 deficient cells. In contrast, genes involved in ribosome biogenesis and mRNA processing were upregulated in multiple cell types. In addition, we observed cell type-specific effects. For example, genes and proteins involved in glutathione synthesis, such as the glutamate-cysteine ligase subunits GCLC and GCLM, were downregulated specifically in lymphoblastoid cells. We provide a web application that enables access to all results generated in this study at https://apps.embl.de/ngly1browser . This resource will guide future studies of NGLY1 deficiency in directions that are most relevant to patients. Graphical Abstract: