Yuan Tian1,2, Mo-Xian Chen2,3, Jing-Fang Yang4, H H K Achala4, Bei Gao3, Ge-Fei Hao4, Guang-Fu Yang4, Zhi-Yong Dian5, Qi-Juan Hu2, Di Zhang3, Jianhua Zhang6,7, Ying-Gao Liu8. 1. State Key Laboratory of Crop Biology, College of Life Science, Shandong Agricultural University, Taian, Shandong, China. 2. Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China. 3. School of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong. 4. Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, 430079, China. 5. Yongyi Biotechnology Co. Ltd, Guangzhou, China. 6. Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China. jzhang@hkbu.edu.hk. 7. Department of Biology, Hong Kong Baptist University and State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, Hong Kong. jzhang@hkbu.edu.hk. 8. State Key Laboratory of Crop Biology, College of Life Science, Shandong Agricultural University, Taian, Shandong, China. liuyg@sdau.edu.cn.
Abstract
MAIN CONCLUSION: This study systematically identifies plant SYF2/NTC31/p29 genes from 62 plant species by a combinatory bioinformatics approach, revealing the importance of this gene family in phylogenetics, duplication, transcriptional, and post-transcriptional regulation. Alternative splicing is a post-transcriptional regulatory mechanism, which is critical for plant development and stress responses. The entire process is strictly attenuated by a complex of splicing-related proteins, designated splicing factors. Human p29, also referred to as synthetic lethal with cdc forty 2 (SYF2) or the NineTeen complex 31 (NTC31), is a core protein found in the NTC complex of humans and yeast. This splicing factor participates in a variety of biological processes, including DNA damage repair, control of the cell cycle, splicing, and tumorigenesis. However, its function in plants has been seldom reported. Thus, we have systematically identified 89 putative plant SYF2s from 62 plant species among the deposited entries in the Phytozome database. The phylogenetic relationships and evolutionary history among these plant SYF2s were carefully examined. The results revealed that plant SYF2s exhibited distinct patterns regarding their gene structure, promoter sequences, and expression levels, suggesting their functional diversity in response to developmental cues or stress treatments. Although local duplication events, such as tandem duplication and retrotransposition, were found among several plant species, most of the plant species contained only one copy of SYF2, suggesting the existence of additional mechanisms to confer duplication resistance. Further investigation using the model dicot and monocot representatives Arabidopsis and rice SYF2s indicated that the splicing pattern and resulting protein isoforms might play an alternative role in the functional diversity.
MAIN CONCLUSION: This study systematically identifies plant SYF2/NTC31/p29 genes from 62 plant species by a combinatory bioinformatics approach, revealing the importance of this gene family in phylogenetics, duplication, transcriptional, and post-transcriptional regulation. Alternative splicing is a post-transcriptional regulatory mechanism, which is critical for plant development and stress responses. The entire process is strictly attenuated by a complex of splicing-related proteins, designated splicing factors. Human p29, also referred to as synthetic lethal with cdc forty 2 (SYF2) or the NineTeen complex 31 (NTC31), is a core protein found in the NTC complex of humans and yeast. This splicing factor participates in a variety of biological processes, including DNA damage repair, control of the cell cycle, splicing, and tumorigenesis. However, its function in plants has been seldom reported. Thus, we have systematically identified 89 putative plant SYF2s from 62 plant species among the deposited entries in the Phytozome database. The phylogenetic relationships and evolutionary history among these plant SYF2s were carefully examined. The results revealed that plant SYF2s exhibited distinct patterns regarding their gene structure, promoter sequences, and expression levels, suggesting their functional diversity in response to developmental cues or stress treatments. Although local duplication events, such as tandem duplication and retrotransposition, were found among several plant species, most of the plant species contained only one copy of SYF2, suggesting the existence of additional mechanisms to confer duplication resistance. Further investigation using the model dicot and monocot representatives Arabidopsis and rice SYF2s indicated that the splicing pattern and resulting protein isoforms might play an alternative role in the functional diversity.
Entities:
Keywords:
Alternative splicing; Gene expression; Gene family; Phylogenetics; Plants; Promoter
Authors: Marlies Löscher; Klaus Fortschegger; Gustav Ritter; Martina Wostry; Regina Voglauer; Johannes A Schmid; Steven Watters; A Jennifer Rivett; Paul Ajuh; Angus I Lamond; Hermann Katinger; Johannes Grillari Journal: Biochem J Date: 2005-06-01 Impact factor: 3.857
Authors: Mau Sun Chang; Chiung Ya Chen; Hung I Yeh; Chi Chen Fan; Chang Jen Huang; Yuh Cheng Yang Journal: Biochem Biophys Res Commun Date: 2002-11-29 Impact factor: 3.575