Department of Forestry and Natural Resources, Purdue University, Hardwood Tree Improvement and Regeneration Center (HTIRC), 715 West State Street, West Lafayette, IN 47907, USA.
USDA Forest Service, Northern Research Station, HTIRC, 715 West State Street, West Lafayette, IN 47907, USA.
Tree Physiol. 2018 Jun 1;38(6):877-894. doi: 10.1093/treephys/tpx175.
Cutting propagation plays a large role in the forestry and horticulture industries where superior genotypes need to be clonally multiplied. Integral to this process is the ability of cuttings to form adventitious roots. Recalcitrance to adventitious root development is a serious hurdle for many woody plant propagation systems including black walnut (Juglans nigra L.), an economically valuable species. The inability of black walnut to reliably form adventitious roots limits propagation of superior genotypes. Adventitious roots originate from different locations, and root induction is controlled by many environmental and endogenous factors. At the molecular level, however, the regulation of adventitious root formation is still poorly understood. In order to elucidate the transcriptional changes during adventitious root development in black walnut, we used quantitative real-time polymerase chain reaction to measure the expression of nine key genes regulating root formation in other species. Using our previously developed spatially explicit timeline of adventitious root development in black walnut softwood cuttings, we optimized a laser capture microdissection protocol to isolate RNA from cortical, phloem fiber and phloem parenchyma cells throughout adventitious root formation. Laser capture microdissection permitted high-resolution, site-specific analysis of gene expression that differentiated between participatory and non-participatory root progenitor cells. Results indicated mRNA abundance was altered in all nine rooting-related genes in response to auxin treatment in both juvenile and mature cuttings. SCARECROW LIKE-1 (SCL) had the greatest change in expression in juvenile rooting-competent cells at days 16 and 18, with a 24- and 23-fold increase relative to day 0, respectively. Tissues not linked to root organogenesis had little change in SCL expression at similar time points. AUXIN RESPONSE FACTOR (ARF)6 and ARF8 as well as SHORTROOT expression also increased 2- to 4-fold in rooting-competent tissue. The greatest transcript abundance in rooting-competent cuttings was restricted to root progenitor cells, while recalcitrant cuttings had a diffuse mRNA signal among tissue types.
组织培养在林业和园艺产业中起着重要作用,需要通过无性繁殖来繁殖优良基因型。组织培养的一个重要组成部分是插条形成不定根的能力。许多木本植物繁殖系统,包括黑胡桃( Juglans nigra L. ),对不定根发育的抗性是一个严重的障碍。黑胡桃不能可靠地形成不定根,限制了优良基因型的繁殖。不定根起源于不同的部位,根的诱导受许多环境和内源性因素的控制。然而,在分子水平上,不定根形成的调控机制仍知之甚少。为了阐明黑胡桃不定根发育过程中的转录变化,我们使用定量实时聚合酶链反应来测量调节其他物种根形成的九个关键基因的表达。利用我们之前开发的黑胡桃软木插条不定根发育时空明确切的时间线,我们优化了一种激光捕获显微解剖方案,以分离不定根形成过程中皮质、韧皮纤维和韧皮薄壁细胞的 RNA。激光捕获显微解剖允许对参与和不参与根原细胞的基因表达进行高分辨率、特定部位的分析。结果表明,在幼龄和成熟插条中,所有九个与生根相关的基因在生长素处理下的 mRNA 丰度都发生了改变。在第 16 天和第 18 天,幼龄生根能力细胞中 SCARECROW LIKE-1(SCL)的表达变化最大,分别比第 0 天增加了 24 倍和 23 倍。在类似的时间点,与根器官发生无关的组织中 SCL 的表达变化很小。AUXIN RESPONSE FACTOR(ARF)6 和 ARF8 以及 SHORTROOT 的表达也在生根能力组织中增加了 2 到 4 倍。在生根能力强的插条中,最大的转录丰度仅限于根原细胞,而抗性插条在组织类型之间具有弥散的 mRNA 信号。