A comprehensive structural, biochemical and biological profiling of the human NUDIX hydrolase family
(2017) In Nature Communications 8(1).- Abstract
The NUDIX enzymes are involved in cellular metabolism and homeostasis, as well as mRNA processing. Although highly conserved throughout all organisms, their biological roles and biochemical redundancies remain largely unclear. To address this, we globally resolve their individual properties and inter-relationships. We purify 18 of the human NUDIX proteins and screen 52 substrates, providing a substrate redundancy map. Using crystal structures, we generate sequence alignment analyses revealing four major structural classes. To a certain extent, their substrate preference redundancies correlate with structural classes, thus linking structure and activity relationships. To elucidate interdependence among the NUDIX hydrolases, we pairwise... (More)
The NUDIX enzymes are involved in cellular metabolism and homeostasis, as well as mRNA processing. Although highly conserved throughout all organisms, their biological roles and biochemical redundancies remain largely unclear. To address this, we globally resolve their individual properties and inter-relationships. We purify 18 of the human NUDIX proteins and screen 52 substrates, providing a substrate redundancy map. Using crystal structures, we generate sequence alignment analyses revealing four major structural classes. To a certain extent, their substrate preference redundancies correlate with structural classes, thus linking structure and activity relationships. To elucidate interdependence among the NUDIX hydrolases, we pairwise deplete them generating an epistatic interaction map, evaluate cell cycle perturbations upon knockdown in normal and cancer cells, and analyse their protein and mRNA expression in normal and cancer tissues. Using a novel FUSION algorithm, we integrate all data creating a comprehensive NUDIX enzyme profile map, which will prove fundamental to understanding their biological functionality.
(Less)
- author
- publishing date
- 2017-11-16
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- A549 Cells, Cell Line, Cell Line, Tumor, Gene Expression Profiling/methods, Gene Expression Regulation, Enzymologic, Gene Expression Regulation, Neoplastic, Gene Regulatory Networks, Humans, MCF-7 Cells, Multigene Family, Phylogeny, Pyrophosphatases/classification, RNA Interference, Substrate Specificity
- in
- Nature Communications
- volume
- 8
- issue
- 1
- article number
- 1541
- publisher
- Nature Publishing Group
- external identifiers
-
- scopus:85034433549
- pmid:29142246
- ISSN
- 2041-1723
- DOI
- 10.1038/s41467-017-01642-w
- language
- English
- LU publication?
- no
- id
- 7f0e46e8-2b2e-477e-8846-fe75d419d5b0
- date added to LUP
- 2019-04-30 07:52:49
- date last changed
- 2024-08-06 14:22:46
@article{7f0e46e8-2b2e-477e-8846-fe75d419d5b0, abstract = {{<p>The NUDIX enzymes are involved in cellular metabolism and homeostasis, as well as mRNA processing. Although highly conserved throughout all organisms, their biological roles and biochemical redundancies remain largely unclear. To address this, we globally resolve their individual properties and inter-relationships. We purify 18 of the human NUDIX proteins and screen 52 substrates, providing a substrate redundancy map. Using crystal structures, we generate sequence alignment analyses revealing four major structural classes. To a certain extent, their substrate preference redundancies correlate with structural classes, thus linking structure and activity relationships. To elucidate interdependence among the NUDIX hydrolases, we pairwise deplete them generating an epistatic interaction map, evaluate cell cycle perturbations upon knockdown in normal and cancer cells, and analyse their protein and mRNA expression in normal and cancer tissues. Using a novel FUSION algorithm, we integrate all data creating a comprehensive NUDIX enzyme profile map, which will prove fundamental to understanding their biological functionality.</p>}}, author = {{Carreras-Puigvert, Jordi and Zitnik, Marinka and Jemth, Ann-Sofie and Carter, Megan and Unterlass, Judith E and Hallström, Björn and Loseva, Olga and Karem, Zhir and Calderón-Montaño, José Manuel and Lindskog, Cecilia and Edqvist, Per-Henrik and Matuszewski, Damian J and Ait Blal, Hammou and Berntsson, Ronnie P A and Häggblad, Maria and Martens, Ulf and Studham, Matthew and Lundgren, Bo and Wählby, Carolina and Sonnhammer, Erik L L and Lundberg, Emma and Stenmark, Pål and Zupan, Blaz and Helleday, Thomas}}, issn = {{2041-1723}}, keywords = {{A549 Cells; Cell Line; Cell Line, Tumor; Gene Expression Profiling/methods; Gene Expression Regulation, Enzymologic; Gene Expression Regulation, Neoplastic; Gene Regulatory Networks; Humans; MCF-7 Cells; Multigene Family; Phylogeny; Pyrophosphatases/classification; RNA Interference; Substrate Specificity}}, language = {{eng}}, month = {{11}}, number = {{1}}, publisher = {{Nature Publishing Group}}, series = {{Nature Communications}}, title = {{A comprehensive structural, biochemical and biological profiling of the human NUDIX hydrolase family}}, url = {{http://dx.doi.org/10.1038/s41467-017-01642-w}}, doi = {{10.1038/s41467-017-01642-w}}, volume = {{8}}, year = {{2017}}, }