Literature DB >> 27456931

Increased Ubqln2 expression causes neuron death in transgenic rats.

Bo Huang1, Qinxue Wu1, Hongxia Zhou2, Cao Huang3, Xu-Gang Xia4.   

Abstract

Pathogenic mutation of ubiquilin 2 (UBQLN2) causes neurodegeneration in amyotrophic lateral sclerosis and frontotemporal lobar degeneration. How UBQLN2 mutations cause the diseases is not clear. While over-expression of UBQLN2 with pathogenic mutation causes neuron death in rodent models, deletion of the Ubqln2 in rats has no effect on neuronal function. Previous findings in animal models suggest that UBQLN2 mutations cause the diseases mainly through a gain rather than a loss of functions. To examine whether the toxic gain in UBQLN2 mutation is related to the enhancement of UBQLN2 functions, we created new transgenic rats over-expressing wild-type human UBQLN2. Considering that human UBQLN2 may not function properly in the rat genome, we also created transgenic rats over-expressing rat's own Ubqln2. When over-expressed in rats, both human and rat wild-type Ubqln2 caused neuronal death and spatial learning deficits, the pathologies that were indistinguishable from those observed in mutant UBQLN2 transgenic rats. Over-expressed wild-type UBQLN2 formed protein inclusions attracting the autophagy substrate sequestosome-1 and the proteasome component 26S proteasome regulatory subunit 7. These findings suggest that excess UBQLN2 is toxic rather than protective to neurons and that the enhancement of UBQLN2 functions is involved in UBQLN2 pathogenesis. Pathogenic mutation in ubiquilin 2 (UBQLN2) causes neurodegeneration in ALS and FTLD. Studies in rodent models suggest a gain of toxic function in mutant UBQLN2. We created new transgenic rats as a relevant model and examined whether enhancing wild-type UBQLN2 expression is implicated in the pathogenesis of mutant UBQLN2. We observed that over-expression of human or rat wild-type Ubqln2 caused protein aggregation and neuronal death in transgenic rats. Our findings suggest that excess UBQLN2 is toxic rather than protective to neurons and that uncontrolled enhancement of UBQLN2 function is involved in UBQLN2 pathogenesis. Read the Editorial Highlight for this article on page 159.
© 2016 International Society for Neurochemistry.

Entities:  

Keywords:  zzm321990ALSzzm321990; zzm321990FTLDzzm321990; Rpt1; Ubqln2; p62; rats

Mesh:

Substances:

Year:  2016        PMID: 27456931      PMCID: PMC5117623          DOI: 10.1111/jnc.13748

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  27 in total

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3.  UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosis.

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Journal:  Neurobiol Aging       Date:  2012-06-19       Impact factor: 4.673

4.  TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration.

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7.  Entorhinal cortical neurons are the primary targets of FUS mislocalization and ubiquitin aggregation in FUS transgenic rats.

Authors:  Cao Huang; Jianbin Tong; Fangfang Bi; Qinxue Wu; Bo Huang; Hongxia Zhou; Xu-Gang Xia
Journal:  Hum Mol Genet       Date:  2012-07-23       Impact factor: 6.150

8.  ubiquilin antagonizes presenilin and promotes neurodegeneration in Drosophila.

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9.  FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

Authors:  Cao Huang; Hongxia Zhou; Jianbin Tong; Han Chen; Yong-Jian Liu; Dian Wang; Xiaotao Wei; Xu-Gang Xia
Journal:  PLoS Genet       Date:  2011-03-03       Impact factor: 5.917

10.  Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.

Authors:  Han-Xiang Deng; Wenjie Chen; Seong-Tshool Hong; Kym M Boycott; George H Gorrie; Nailah Siddique; Yi Yang; Faisal Fecto; Yong Shi; Hong Zhai; Hujun Jiang; Makito Hirano; Evadnie Rampersaud; Gerard H Jansen; Sandra Donkervoort; Eileen H Bigio; Benjamin R Brooks; Kaouther Ajroud; Robert L Sufit; Jonathan L Haines; Enrico Mugnaini; Margaret A Pericak-Vance; Teepu Siddique
Journal:  Nature       Date:  2011-08-21       Impact factor: 49.962

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  14 in total

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Review 2.  Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration.

Authors:  C Maurel; A Dangoumau; S Marouillat; C Brulard; A Chami; R Hergesheimer; P Corcia; H Blasco; C R Andres; P Vourc'h
Journal:  Mol Neurobiol       Date:  2018-01-10       Impact factor: 5.590

3.  Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS-FTD-linked UBQLN2 mutations.

Authors:  Nhat T T Le; Lydia Chang; Irina Kovlyagina; Polymnia Georgiou; Nathaniel Safren; Kerstin E Braunstein; Mark D Kvarta; Adam M Van Dyke; Tara A LeGates; Thomas Philips; Brett M Morrison; Scott M Thompson; Adam C Puche; Todd D Gould; Jeffrey D Rothstein; Philip C Wong; Mervyn J Monteiro
Journal:  Proc Natl Acad Sci U S A       Date:  2016-11-09       Impact factor: 11.205

Review 4.  Modelling amyotrophic lateral sclerosis in rodents.

Authors:  Tiffany W Todd; Leonard Petrucelli
Journal:  Nat Rev Neurosci       Date:  2022-03-08       Impact factor: 34.870

5.  Mutation-dependent aggregation and toxicity in a Drosophila model for UBQLN2-associated ALS.

Authors:  Sang Hwa Kim; Shannon G Stiles; Joseph M Feichtmeier; Nandini Ramesh; Lihong Zhan; Mark A Scalf; Lloyd M Smith; Udai Bhan Pandey; Randal S Tibbetts
Journal:  Hum Mol Genet       Date:  2018-01-15       Impact factor: 6.150

Review 6.  Structure, dynamics and functions of UBQLNs: at the crossroads of protein quality control machinery.

Authors:  Tongyin Zheng; Yiran Yang; Carlos A Castañeda
Journal:  Biochem J       Date:  2020-09-30       Impact factor: 3.857

7.  Mutant UBQLN2 promotes toxicity by modulating intrinsic self-assembly.

Authors:  Lisa M Sharkey; Nathaniel Safren; Amit S Pithadia; Julia E Gerson; Mark Dulchavsky; Svetlana Fischer; Ronak Patel; Gabrielle Lantis; Naila Ashraf; John H Kim; Alia Meliki; Eiko N Minakawa; Sami J Barmada; Magdalena I Ivanova; Henry L Paulson
Journal:  Proc Natl Acad Sci U S A       Date:  2018-10-17       Impact factor: 11.205

8.  ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import.

Authors:  Brian C Lin; Trong H Phung; Nicole R Higgins; Jessie E Greenslade; Miguel A Prado; Daniel Finley; Mariusz Karbowski; Brian M Polster; Mervyn J Monteiro
Journal:  Hum Mol Genet       Date:  2021-06-17       Impact factor: 6.150

9.  Impaired 26S Proteasome Assembly Precedes Neuronal Loss in Mutant UBQLN2 Rats.

Authors:  Wenjuan Zhang; Bo Huang; Limo Gao; Cao Huang
Journal:  Int J Mol Sci       Date:  2021-04-21       Impact factor: 5.923

Review 10.  Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand.

Authors:  Nandini Ramesh; Udai Bhan Pandey
Journal:  Front Mol Neurosci       Date:  2017-08-22       Impact factor: 5.639

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