Dorsal telencephalon-specific Nprl2- and Nprl3-knockout mice: novel mouse models for GATORopathy. Issue 9 (20th November 2021)
- Record Type:
- Journal Article
- Title:
- Dorsal telencephalon-specific Nprl2- and Nprl3-knockout mice: novel mouse models for GATORopathy. Issue 9 (20th November 2021)
- Main Title:
- Dorsal telencephalon-specific Nprl2- and Nprl3-knockout mice: novel mouse models for GATORopathy
- Authors:
- Ishida, Saeko
Zhao, Di
Sawada, Yuta
Hiraoka, Yuichi
Mashimo, Tomoji
Tanaka, Kohichi - Abstract:
- Abstract: The most frequent genetic cause of focal epilepsies is variations in the GAP activity toward RAGs 1 complex genes DEP domain containing 5 ( DEPDC5 ), nitrogen permease regulator 2-like protein ( NPRL2 ) and nitrogen permease regulator 3-like protein ( NPRL3 ). Because these variations are frequent and associated with a broad spectrum of focal epilepsies, a unique pathology categorized as GATORopathy can be conceptualized. Animal models recapitulating the clinical features of patients are essential to decipher GATORopathy. Although several genetically modified animal models recapitulate DEPDC5 -related epilepsy, no models have been reported for NPRL2 - or NPRL3 -related epilepsies. Here, we conditionally deleted Nprl2 and Nprl3 from the dorsal telencephalon in mice [ Emx1 cre/+ ; Nprl2 f/f ( Nprl2 -cKO) and Emx1 cre/+ ; Nprl3 f/f ( Nprl3 -cKO)] and compared their phenotypes with Nprl2 +/ −, Nprl3 +/ − and Emx1 cre/+ ; Depdc5 f/f ( Depdc5 -cKO) mice. Nprl2 -cKO and Nprl3 -cKO mice recapitulated the major abnormal features of patients—spontaneous seizures, and dysmorphic enlarged neuronal cells with increased mechanistic target of rapamycin complex 1 signaling—similar to Depdc5 -cKO mice. Chronic postnatal rapamycin administration dramatically prolonged the survival period and inhibited seizure occurrence but not enlarged neuronal cells in Nprl2 -cKO and Nprl3 -cKO mice. However, the benefit of rapamycin after withdrawal was less durable in Nprl2 - and Nprl3 -cKO miceAbstract: The most frequent genetic cause of focal epilepsies is variations in the GAP activity toward RAGs 1 complex genes DEP domain containing 5 ( DEPDC5 ), nitrogen permease regulator 2-like protein ( NPRL2 ) and nitrogen permease regulator 3-like protein ( NPRL3 ). Because these variations are frequent and associated with a broad spectrum of focal epilepsies, a unique pathology categorized as GATORopathy can be conceptualized. Animal models recapitulating the clinical features of patients are essential to decipher GATORopathy. Although several genetically modified animal models recapitulate DEPDC5 -related epilepsy, no models have been reported for NPRL2 - or NPRL3 -related epilepsies. Here, we conditionally deleted Nprl2 and Nprl3 from the dorsal telencephalon in mice [ Emx1 cre/+ ; Nprl2 f/f ( Nprl2 -cKO) and Emx1 cre/+ ; Nprl3 f/f ( Nprl3 -cKO)] and compared their phenotypes with Nprl2 +/ −, Nprl3 +/ − and Emx1 cre/+ ; Depdc5 f/f ( Depdc5 -cKO) mice. Nprl2 -cKO and Nprl3 -cKO mice recapitulated the major abnormal features of patients—spontaneous seizures, and dysmorphic enlarged neuronal cells with increased mechanistic target of rapamycin complex 1 signaling—similar to Depdc5 -cKO mice. Chronic postnatal rapamycin administration dramatically prolonged the survival period and inhibited seizure occurrence but not enlarged neuronal cells in Nprl2 -cKO and Nprl3 -cKO mice. However, the benefit of rapamycin after withdrawal was less durable in Nprl2 - and Nprl3 -cKO mice compared with Depdc5 -cKO mice. Further studies using these conditional knockout mice will be useful for understanding GATORopathy and for the identification of novel therapeutic targets. … (more)
- Is Part Of:
- Human molecular genetics. Volume 31:Issue 9(2022)
- Journal:
- Human molecular genetics
- Issue:
- Volume 31:Issue 9(2022)
- Issue Display:
- Volume 31, Issue 9 (2022)
- Year:
- 2022
- Volume:
- 31
- Issue:
- 9
- Issue Sort Value:
- 2022-0031-0009-0000
- Page Start:
- 1519
- Page End:
- 1530
- Publication Date:
- 2021-11-20
- Subjects:
- Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8 - Journal URLs:
- http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/hmg/ddab337 ↗
- Languages:
- English
- ISSNs:
- 0964-6906
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
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- 21415.xml