Author
Listed:
- Greta Pintacuda
(Stanley Center at Broad Institute of MIT and Harvard
Harvard University)
- Frederik H. Lassen
(Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital
University of Oxford)
- Yu-Han H. Hsu
(Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital)
- April Kim
(Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital
Johns Hopkins University)
- Jacqueline M. Martín
(Stanley Center at Broad Institute of MIT and Harvard
Harvard University)
- Edyta Malolepsza
(Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital)
- Justin K. Lim
(Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital
Massachusetts Institute of Technology)
- Nadine Fornelos
(Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital)
- Kevin C. Eggan
(Stanley Center at Broad Institute of MIT and Harvard
Harvard University)
- Kasper Lage
(Stanley Center at Broad Institute of MIT and Harvard
Massachusetts General Hospital
Institute of Biological Psychiatry, Mental Health Centre Sct. Hans, Mental Health Services Copenhagen)
Abstract
Combining genetic and cell-type-specific proteomic datasets can generate biological insights and therapeutic hypotheses, but a technical and statistical framework for such analyses is lacking. Here, we present an open-source computational tool called Genoppi (lagelab.org/genoppi) that enables robust, standardized, and intuitive integration of quantitative proteomic results with genetic data. We use Genoppi to analyze 16 cell-type-specific protein interaction datasets of four proteins (BCL2, TDP-43, MDM2, PTEN) involved in cancer and neurological disease. Through systematic quality control of the data and integration with published protein interactions, we show a general pattern of both cell-type-independent and cell-type-specific interactions across three cancer cell types and one human iPSC-derived neuronal cell type. Furthermore, through the integration of proteomic and genetic datasets in Genoppi, our results suggest that the neuron-specific interactions of these proteins are mediating their genetic involvement in neurodegenerative diseases. Importantly, our analyses suggest that human iPSC-derived neurons are a relevant model system for studying the involvement of BCL2 and TDP-43 in amyotrophic lateral sclerosis.
Suggested Citation
Greta Pintacuda & Frederik H. Lassen & Yu-Han H. Hsu & April Kim & Jacqueline M. Martín & Edyta Malolepsza & Justin K. Lim & Nadine Fornelos & Kevin C. Eggan & Kasper Lage, 2021.
"Genoppi is an open-source software for robust and standardized integration of proteomic and genetic data,"
Nature Communications, Nature, vol. 12(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-22648-5
DOI: 10.1038/s41467-021-22648-5
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