Department of Botany, University of British Columbia, Vancouver, BC, Canada.
Graduate School of Science and Engineering, Saitama University, Saitama, Japan.
Plant J. 2020 Jan;101(2):293-309. doi: 10.1111/tpj.14541. Epub 2019 Nov 11.
The transcription factor KNOTTED ARABIDOPSIS THALIANA7 (KNAT7) is a Class II KNOTTED1-like homeobox (KNOX2) gene that, in interfascicular fibres, acts as a negative regulator of secondary cell wall biosynthesis. In addition, knat7 loss-of-function mutants display an irregular xylem (irx) phenotype, suggesting a potential positive regulatory role in xylem vessel secondary cell wall deposition. Although our understanding of the role of KNAT7 is evolving, the function(s) of the closely related KNOX2 genes, KNAT3, KNAT4, and KNAT5, in secondary wall formation still remain unclear. We found that all four Arabidopsis KNOX2 genes were expressed in the inflorescence stems. However, only the knat3 knat7 double mutants showed a phenotype, displaying an enhanced irx phenotypes relative to the single mutants, as well as decreased interfascicular fibre cell wall thickness. Moreover, knat3 knat7 double mutants had reduced stem tensile and flexural strength compared with wild-type and single mutants. In contrast, KNAT3 overexpression resulted in thicker interfascicular fibre secondary cell walls in inflorescence stems, suggesting a potential positive regulation in interfascicular fibre secondary wall development. This work identifies KNAT3 as a potential transcriptional activator working together with KNAT7 to promote secondary cell wall biosynthesis in xylem vessels, while concurrently acting antagonistically with KNAT7 to influence secondary wall formation in interfascicular fibres.
转录因子 KNOTTED ARABIDOPSIS THALIANA7(KNAT7)是一个 II 类 KNOTTED1 类同源盒(KNOX2)基因,在束间纤维中,作为次生细胞壁生物合成的负调控因子。此外,knat7 功能丧失突变体表现出不规则木质部(irx)表型,这表明其在木质部导管次生细胞壁沉积中可能具有正向调控作用。尽管我们对 KNAT7 功能的理解在不断发展,但与 KNAT7 密切相关的 KNOX2 基因 KNAT3、KNAT4 和 KNAT5 在次生壁形成中的功能仍不清楚。我们发现拟南芥的四个 KNOX2 基因都在花序茎中表达。然而,只有 knat3 knat7 双突变体表现出表型,与单突变体相比,irx 表型增强,束间纤维细胞壁厚度降低。此外,knat3 knat7 双突变体的茎拉伸和弯曲强度比野生型和单突变体都低。相比之下,KNAT3 的过表达导致花序茎中束间纤维次生细胞壁变厚,这表明其在束间纤维次生细胞壁发育中可能具有正向调控作用。这项工作确定了 KNAT3 是一个潜在的转录激活因子,与 KNAT7 一起促进木质部导管的次生细胞壁生物合成,同时与 KNAT7 拮抗作用影响束间纤维的次生壁形成。