2015
DOI: 10.1016/j.plantsci.2015.05.005
|View full text |Cite
|
Sign up to set email alerts
|

The KNOTTED-like genes of peach (Prunus persica L. Batsch) are differentially expressed during drupe growth and the class 1 KNOPE1 contributes to mesocarp development

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
3
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
5

Relationship

1
4

Authors

Journals

citations
Cited by 5 publications
(3 citation statements)
references
References 71 publications
0
3
0
Order By: Relevance
“…In addition, KNOPE1 is expressed in cortex and procambium at the primary growth stage of stems and prevents the lignification of primary stems by inhibiting ligninrelated genes (Testone et al, 2012). Subsequent studies found that KNOPE1 could inhibit the expression of PpGA3ox1 to affect gibberellin(GA) homeostasis, thereby regulating peel differentiation (Testone et al, 2015). Peach KNOPE3 (belonging to KNOX class II) may be involved in the regulation of sugar transport processes (Testone et al, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…In addition, KNOPE1 is expressed in cortex and procambium at the primary growth stage of stems and prevents the lignification of primary stems by inhibiting ligninrelated genes (Testone et al, 2012). Subsequent studies found that KNOPE1 could inhibit the expression of PpGA3ox1 to affect gibberellin(GA) homeostasis, thereby regulating peel differentiation (Testone et al, 2015). Peach KNOPE3 (belonging to KNOX class II) may be involved in the regulation of sugar transport processes (Testone et al, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…The interaction of them affects phytohormone regulation that is related to plant development (Niu & Fu 2022). The heterodimer modulates phytohormone by activating cytokinin and repressing gibberellin (Tadege 2013;Testone et al 2015;Marsch-Martínez & de Folter 2016), which correlates to shoot development (Wybouw & De Rybel 2019;Arro et al 2019). Not only for shoot development, but also KNOX protein linked up to the lignification process in dicot and monocot plants (Townsley et al 2013;Xu et al 2019), the diversity of leaf shape (Gao et al 2015;Wang et al 2022), and a necessary role in starchy storage organs (Dong et al 2019;Rüscher et al 2021).…”
Section: Protein Modelling Of Poh1 Protein and Its Domain Functionmentioning
confidence: 99%
“…homeobox 12 (ATHB12) (Hur et al, 2015), NGATHA (NGA) (Ballester et al, 2015), ABCB19 (an ATP‐binding cassette membrane protein required for polar auxin transport) (Wu et al, 2016), myosins (motor proteins) (Peremyslov et al, 2015), BRI1‐EMS‐SUPPRESSOR1 (BES1) (Jiang et al, 2015), RLP44 (a receptor‐like protein) (Wolf et al, 2014), PSKR1 (a leucine‐rich repeat receptor kinase for phytosulfokine) (Ladwig et al, 2015), Cotton ( Gossypium hirsutum L.) Golgi‐Related 2 and 3 (CGR2 and ‐3) (Weraduwage et al, 2016), SPIRAL1 (SPR1, the microtubule plus‐end tracking protein) (Nakajima et al, 2004; Galva et al, 2014), augmin complex (Liu et al, 2014), SNARE (soluble N‐ethylmaleimide‐sensitive factor attachment protein receptor)/AtVAM3/AtVTI11/SYP121/122 (Yano et al, 2003; Löfke et al, 2015), SEC11/KEULE (Karnik et al, 2015), ZmABA8ox1b (Li et al, 2016), and ADP‐ribosylation factor (ZmArf2) (Wang et al, 2016a). By contrast, several factors were shown to control organ growth by negatively regulating cell expansion, including BIGPETALp (BPEp), RPT2a (Szécsi et al, 2006; Kurepa et al, 2009; Sonoda et al, 2009), MULTIPASS (OsMPS, an R2R3‐type MYB transcription factor [TF]) (Schmidt et al, 2013), PEROXIDASE71 (AtPRX71) (Raggi et al, 2015), Sl‐IAA17 (Aux and IAA transcriptional repressor) (Su et al, 2014), KNOPE1 (KNOTTED‐like) (Testone et al, 2015), AtKINESIN‐13A (AtKIN13A) (Fujikura et al, 2014), and rapid alkalinization factor (RALF) (Pearce et al, 2001; Bergonci et al, 2014).…”
mentioning
confidence: 99%