The nuclear pore Y-complex functions as a platform for transcriptional regulation of FLOWERING LOCUS C in Arabidopsis

Author:

Huang Penghui12ORCID,Zhang Xiaomei2ORCID,Cheng Zhiyuan3ORCID,Wang Xu4ORCID,Miao Yuchen5ORCID,Huang Guowen6ORCID,Fu Yong-Fu2ORCID,Feng Xianzhong13ORCID

Affiliation:

1. Zhejiang Lab, Research Institute of Intelligent Computing , Hangzhou 310012 , China

2. MARA Key Laboratory of Soybean Biology (Beijing), State Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences , Beijing 100081 , China

3. CAS Key Laboratory of Soybean Molecular Design Breeding, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences , Changchun 130102 , China

4. Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agricultural Sciences at Weifang , Weifang, Shandong 261325 , China

5. State Key Laboratory of Crop Stress Adaptation and Improvement, School of Life Sciences, Henan University , Kaifeng 475004 , China

6. Department of Biological Sciences and Chemical Engineering, Hunan University of Science and Engineering , Yongzhou 425100, Hunan , China

Abstract

Abstract The nuclear pore complex (NPC) has multiple functions beyond the nucleo-cytoplasmic transport of large molecules. Subnuclear compartmentalization of chromatin is critical for gene expression in animals and yeast. However, the mechanism by which the NPC regulates gene expression is poorly understood in plants. Here we report that the Y-complex (Nup107–160 complex, a subcomplex of the NPC) self-maintains its nucleoporin homeostasis and modulates FLOWERING LOCUS C (FLC) transcription via changing histone modifications at this locus. We show that Y-complex nucleoporins are intimately associated with FLC chromatin through their interactions with histone H2A at the nuclear membrane. Fluorescence in situ hybridization assays revealed that Nup96, a Y-complex nucleoporin, enhances FLC positioning at the nuclear periphery. Nup96 interacted with HISTONE DEACETYLASE 6 (HDA6), a key repressor of FLC expression via histone modification, at the nuclear membrane to attenuate HDA6-catalyzed deposition at the FLC locus and change histone modifications. Moreover, we demonstrate that Y-complex nucleoporins interact with RNA polymerase II to increase its occupancy at the FLC locus, facilitating transcription. Collectively, our findings identify an attractive mechanism for the Y-complex in regulating FLC expression via tethering the locus at the nuclear periphery and altering its histone modification.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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