Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy
Via whole-exome sequencing, we identified rare autosomal-recessive variants in UBA5 in five children from four unrelated families affected with a similar pattern of severe intellectual deficiency, microcephaly, movement disorders, and/or early-onset intractable epilepsy. UBA5 encodes the E1-activati...
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
18 August 2016
|
| In: |
The American journal of human genetics
Year: 2016, Volume: 99, Issue: 3, Pages: 695-703 |
| ISSN: | 1537-6605 |
| DOI: | 10.1016/j.ajhg.2016.06.030 |
| Online Access: | Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1016/j.ajhg.2016.06.030 Verlag, kostenfrei, Volltext: https://www.sciencedirect.com/science/article/pii/S0002929716302683?via%3Dihub 
|
| Author Notes: | Estelle Colin, Jens Daniel, Alban Ziegler, Jamal Wakim, Aurora Scrivo, Tobias B. Haack, Salim Khiati, Anne-Sophie Denommé, Patrizia Amati-Bonneau, Majida Charif, Vincent Procaccio, Pascal Reynier, Kyrieckos A. Aleck, Lorenzo D. Botto, Claudia Lena Herper, Charlotte Sophia Kaiser, Rima Nabbout, Sylvie N’Guyen, José Antonio Mora-Lorca, Birgit Assmann, Stine Christ, Thomas Meitinger, Tim M. Strom, Holger Prokisch, Antonio Miranda-Vizuete, Georg F. Hoffmann, Guy Lenaers, Pascale Bomont, Eva Liebau, and Dominique Bonneau |
MARC
| LEADER | 00000caa a2200000 c 4500 | ||
|---|---|---|---|
| 001 | 1568056664 | ||
| 003 | DE-627 | ||
| 005 | 20250206094719.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 180202s2016 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1016/j.ajhg.2016.06.030 |2 doi | |
| 035 | |a (DE-627)1568056664 | ||
| 035 | |a (DE-576)49805666X | ||
| 035 | |a (DE-599)BSZ49805666X | ||
| 035 | |a (OCoLC)1340986263 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rda | ||
| 041 | |a eng | ||
| 084 | |a 33 |2 sdnb | ||
| 100 | 1 | |a Colin, Estelle |e VerfasserIn |0 (DE-588)1151740748 |0 (DE-627)1012258327 |0 (DE-576)498058123 |4 aut | |
| 245 | 1 | 0 | |a Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy |c Estelle Colin, Jens Daniel, Alban Ziegler, Jamal Wakim, Aurora Scrivo, Tobias B. Haack, Salim Khiati, Anne-Sophie Denommé, Patrizia Amati-Bonneau, Majida Charif, Vincent Procaccio, Pascal Reynier, Kyrieckos A. Aleck, Lorenzo D. Botto, Claudia Lena Herper, Charlotte Sophia Kaiser, Rima Nabbout, Sylvie N’Guyen, José Antonio Mora-Lorca, Birgit Assmann, Stine Christ, Thomas Meitinger, Tim M. Strom, Holger Prokisch, Antonio Miranda-Vizuete, Georg F. Hoffmann, Guy Lenaers, Pascale Bomont, Eva Liebau, and Dominique Bonneau |
| 264 | 1 | |c 18 August 2016 | |
| 300 | |a 9 | ||
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
| 338 | |a Online-Ressource |b cr |2 rdacarrier | ||
| 500 | |a Gesehen am 02.02.2018 | ||
| 520 | |a Via whole-exome sequencing, we identified rare autosomal-recessive variants in UBA5 in five children from four unrelated families affected with a similar pattern of severe intellectual deficiency, microcephaly, movement disorders, and/or early-onset intractable epilepsy. UBA5 encodes the E1-activating enzyme of ubiquitin-fold modifier 1 (UFM1), a recently identified ubiquitin-like protein. Biochemical studies of mutant UBA5 proteins and studies in fibroblasts from affected individuals revealed that UBA5 mutations impair the process of ufmylation, resulting in an abnormal endoplasmic reticulum structure. In Caenorhabditis elegans, knockout of uba-5 and of human orthologous genes in the UFM1 cascade alter cholinergic, but not glutamatergic, neurotransmission. In addition, uba5 silencing in zebrafish decreased motility while inducing abnormal movements suggestive of seizures. These clinical, biochemical, and experimental findings support our finding of UBA5 mutations as a pathophysiological cause for early-onset encephalopathies due to abnormal protein ufmylation. | ||
| 700 | 1 | |a Assmann, Birgit |d 1962- |e VerfasserIn |0 (DE-588)112011926 |0 (DE-627)470185953 |0 (DE-576)289718619 |4 aut | |
| 700 | 1 | |a Christ, Stine |d 1983- |e VerfasserIn |0 (DE-588)143694154 |0 (DE-627)653854862 |0 (DE-576)338419810 |4 aut | |
| 700 | 1 | |a Hoffmann, Georg F. |d 1957- |e VerfasserIn |0 (DE-588)115652868 |0 (DE-627)077386116 |0 (DE-576)261230042 |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t The American journal of human genetics |d New York, NY [u.a.] : Cell Press, 1949 |g 99(2016), 3, Seite 695-703 |w (DE-627)269019014 |w (DE-600)1473813-2 |w (DE-576)077662636 |x 1537-6605 |7 nnas |a Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy |
| 773 | 1 | 8 | |g volume:99 |g year:2016 |g number:3 |g pages:695-703 |g extent:9 |a Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy |
| 856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.ajhg.2016.06.030 |x Verlag |x Resolving-System |z kostenfrei |3 Volltext |
| 856 | 4 | 0 | |u https://www.sciencedirect.com/science/article/pii/S0002929716302683?via%3Dihub |x Verlag |z kostenfrei |3 Volltext |
| 951 | |a AR | ||
| 992 | |a 20180202 | ||
| 993 | |a Article | ||
| 994 | |a 2016 | ||
| 998 | |g 115652868 |a Hoffmann, Georg F. |m 115652868:Hoffmann, Georg F. |d 910000 |d 910500 |e 910000PH115652868 |e 910500PH115652868 |k 0/910000/ |k 1/910000/910500/ |p 26 | ||
| 998 | |g 143694154 |a Christ, Stine |m 143694154:Christ, Stine |d 910000 |d 910500 |e 910000PC143694154 |e 910500PC143694154 |k 0/910000/ |k 1/910000/910500/ |p 21 | ||
| 998 | |g 112011926 |a Assmann, Birgit |m 112011926:Assmann, Birgit |d 910000 |d 910500 |e 910000PA112011926 |e 910500PA112011926 |k 0/910000/ |k 1/910000/910500/ |p 20 | ||
| 999 | |a KXP-PPN1568056664 |e 2995072991 | ||
| BIB | |a Y | ||
| SER | |a journal | ||
| JSO | |a {"relHost":[{"part":{"volume":"99","pages":"695-703","text":"99(2016), 3, Seite 695-703","extent":"9","issue":"3","year":"2016"},"origin":[{"publisherPlace":"New York, NY [u.a.] ; New York, NY ; Chicago, Ill.","dateIssuedDisp":"1949-","publisher":"Cell Press ; Elsevier ; Univ. of Chicago Press","dateIssuedKey":"1949"}],"id":{"eki":["269019014"],"zdb":["1473813-2"],"issn":["1537-6605"]},"disp":"Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathyThe American journal of human genetics","recId":"269019014","name":{"displayForm":["American Society of Human Genetics"]},"title":[{"title_sort":"American journal of human genetics","title":"The American journal of human genetics"}],"pubHistory":["1.1949 -"],"language":["eng"],"note":["Gesehen am 28.05.2020"],"type":{"media":"Online-Ressource","bibl":"periodical"},"corporate":[{"display":"American Society of Human Genetics","role":"isb"}]}],"note":["Gesehen am 02.02.2018"],"id":{"eki":["1568056664"],"doi":["10.1016/j.ajhg.2016.06.030"]},"origin":[{"dateIssuedKey":"2016","dateIssuedDisp":"18 August 2016"}],"name":{"displayForm":["Estelle Colin, Jens Daniel, Alban Ziegler, Jamal Wakim, Aurora Scrivo, Tobias B. Haack, Salim Khiati, Anne-Sophie Denommé, Patrizia Amati-Bonneau, Majida Charif, Vincent Procaccio, Pascal Reynier, Kyrieckos A. Aleck, Lorenzo D. Botto, Claudia Lena Herper, Charlotte Sophia Kaiser, Rima Nabbout, Sylvie N’Guyen, José Antonio Mora-Lorca, Birgit Assmann, Stine Christ, Thomas Meitinger, Tim M. Strom, Holger Prokisch, Antonio Miranda-Vizuete, Georg F. Hoffmann, Guy Lenaers, Pascale Bomont, Eva Liebau, and Dominique Bonneau"]},"recId":"1568056664","person":[{"display":"Colin, Estelle","family":"Colin","given":"Estelle","role":"aut"},{"role":"aut","given":"Birgit","family":"Assmann","display":"Assmann, Birgit"},{"given":"Stine","role":"aut","family":"Christ","display":"Christ, Stine"},{"role":"aut","given":"Georg F.","family":"Hoffmann","display":"Hoffmann, Georg F."}],"title":[{"title_sort":"Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy","title":"Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy"}],"type":{"bibl":"article-journal","media":"Online-Ressource"},"language":["eng"],"physDesc":[{"extent":"9 S."}]} | ||
| SRT | |a COLINESTELBIALLELICV1820 | ||