Cargando…

Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms

The ubiquitin‐like modifier (UBL) SUMO (Small Ubiquitin‐Like Modifier) regulates protein function. Structural rather than sequence homology typifies UBL families. However, individual UBL types, such as SUMO, show remarkable sequence conservation. Selection pressure also operates at the SUMO gene cop...

Descripción completa

Detalles Bibliográficos
Autores principales: Hammoudi, Valentin, Vlachakis, Georgios, Schranz, M. Eric, van den Burg, Harrold A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680281/
https://www.ncbi.nlm.nih.gov/pubmed/26934536
http://dx.doi.org/10.1111/nph.13911
_version_ 1783441467557019648
author Hammoudi, Valentin
Vlachakis, Georgios
Schranz, M. Eric
van den Burg, Harrold A.
author_facet Hammoudi, Valentin
Vlachakis, Georgios
Schranz, M. Eric
van den Burg, Harrold A.
author_sort Hammoudi, Valentin
collection PubMed
description The ubiquitin‐like modifier (UBL) SUMO (Small Ubiquitin‐Like Modifier) regulates protein function. Structural rather than sequence homology typifies UBL families. However, individual UBL types, such as SUMO, show remarkable sequence conservation. Selection pressure also operates at the SUMO gene copy number, as increased SUMO levels activate immunity and alter flowering time in Arabidopsis. We show how, despite this selection pressure, the SUMO family has diversified into eight paralogues in Arabidopsis. Relationships between the paralogues were investigated using genome collinearity and gene tree analysis. We show that palaeopolyploidy followed by tandem duplications allowed expansion and then diversification of the SUMO genes. For example, Arabidopsis SUMO5 evolved from the pan‐eudicot palaeohexaploidy event (gamma), which yielded three SUMO copies. Two gamma copies were preserved as archetype SUMOs, suggesting subfunctionalization, whereas the third copy served as a hotspot for SUMO diversification. The Brassicaceae‐specific alpha duplication then caused the duplication of one archetype gamma copy, which, by subfunctionalization, allowed the retention of both SUMO1 and SUMO2. The other archetype gamma copy was simultaneously pseudogenized (SUMO4/6). A tandem duplication of SUMO2 subsequently yielded SUMO3 in the Brassicaceae crown group. SUMO3 potentially neofunctionalized in Arabidopsis, but it is lost in many Brassicaceae. Our advanced methodology allows the study of the birth and fixation of other paralogues in plants.
format Online
Article
Text
id pubmed-6680281
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-66802812019-08-09 Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms Hammoudi, Valentin Vlachakis, Georgios Schranz, M. Eric van den Burg, Harrold A. New Phytol Research The ubiquitin‐like modifier (UBL) SUMO (Small Ubiquitin‐Like Modifier) regulates protein function. Structural rather than sequence homology typifies UBL families. However, individual UBL types, such as SUMO, show remarkable sequence conservation. Selection pressure also operates at the SUMO gene copy number, as increased SUMO levels activate immunity and alter flowering time in Arabidopsis. We show how, despite this selection pressure, the SUMO family has diversified into eight paralogues in Arabidopsis. Relationships between the paralogues were investigated using genome collinearity and gene tree analysis. We show that palaeopolyploidy followed by tandem duplications allowed expansion and then diversification of the SUMO genes. For example, Arabidopsis SUMO5 evolved from the pan‐eudicot palaeohexaploidy event (gamma), which yielded three SUMO copies. Two gamma copies were preserved as archetype SUMOs, suggesting subfunctionalization, whereas the third copy served as a hotspot for SUMO diversification. The Brassicaceae‐specific alpha duplication then caused the duplication of one archetype gamma copy, which, by subfunctionalization, allowed the retention of both SUMO1 and SUMO2. The other archetype gamma copy was simultaneously pseudogenized (SUMO4/6). A tandem duplication of SUMO2 subsequently yielded SUMO3 in the Brassicaceae crown group. SUMO3 potentially neofunctionalized in Arabidopsis, but it is lost in many Brassicaceae. Our advanced methodology allows the study of the birth and fixation of other paralogues in plants. John Wiley and Sons Inc. 2016-03-02 2016-07 /pmc/articles/PMC6680281/ /pubmed/26934536 http://dx.doi.org/10.1111/nph.13911 Text en © 2016 The Authors. New Phytologist © 2016 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hammoudi, Valentin
Vlachakis, Georgios
Schranz, M. Eric
van den Burg, Harrold A.
Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms
title Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms
title_full Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms
title_fullStr Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms
title_full_unstemmed Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms
title_short Whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier SUMO in Angiosperms
title_sort whole‐genome duplications followed by tandem duplications drive diversification of the protein modifier sumo in angiosperms
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680281/
https://www.ncbi.nlm.nih.gov/pubmed/26934536
http://dx.doi.org/10.1111/nph.13911
work_keys_str_mv AT hammoudivalentin wholegenomeduplicationsfollowedbytandemduplicationsdrivediversificationoftheproteinmodifiersumoinangiosperms
AT vlachakisgeorgios wholegenomeduplicationsfollowedbytandemduplicationsdrivediversificationoftheproteinmodifiersumoinangiosperms
AT schranzmeric wholegenomeduplicationsfollowedbytandemduplicationsdrivediversificationoftheproteinmodifiersumoinangiosperms
AT vandenburgharrolda wholegenomeduplicationsfollowedbytandemduplicationsdrivediversificationoftheproteinmodifiersumoinangiosperms