Cell-type-specific transcriptome and histone modification dynamics during cellular reprogramming in the Arabidopsis stomatal lineage

被引:48
|
作者
Lee, Laura R. [1 ]
Wengier, Diego L. [1 ,2 ,3 ]
Bergmann, Dominique C. [1 ,2 ]
机构
[1] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[2] Stanford Univ, HHMI, Stanford, CA 94305 USA
[3] Consejo Nacl Invest Cient & Tecn, Inst Invest Ingn Genet & Biol Mol Dr Hector N Tor, Vuelta Obligado 2490, RA-1428 Caba, Argentina
关键词
reprogramming; H3K27me3; stomata; Arabidopsis; GUARD-CELLS; HOMEODOMAIN PROTEINS; EXPRESSION; FAMA; GENE; DIFFERENTIATION; BIOSYNTHESIS; IDENTITY; LOOP;
D O I
10.1073/pnas.1911400116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Plant cells maintain remarkable developmental plasticity, allowing them to clonally reproduce and to repair tissues following wounding; yet plant cells normally stably maintain consistent identities. Although this capacity was recognized long ago, our mechanistic understanding of the establishment, maintenance, and erasure of cellular identities in plants remains limited. Here, we develop a cell-type-specific reprogramming system that can be probed at the genome-wide scale for alterations in gene expression and histone modifications. We show that relationships among H3K27me3, H3K4me3, and gene expression in single cell types mirror trends from complex tissue, and that H3K27me3 dynamics regulate guard cell identity. Further, upon initiation of reprogramming, guard cells induce H3K27me3-mediated repression of a regulator of wound-induced callus formation, suggesting that cells in intact tissues may have mechanisms to sense and resist inappropriate dedifferentiation. The matched ChIP-sequencing (seq) and RNA-seq datasets created for this analysis also serve as a resource enabling inquiries into the dynamic and global-scale distribution of histone modifications in single cell types in plants.
引用
收藏
页码:21914 / 21924
页数:11
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