A reflux-and-growth mechanism explains oscillatory patterning of lateral root branching sites

Autor: van den Berg, Thea, Yalamanchili, Kavya, de Gernier, Hugues, Santos Teixeira, Joana, Beeckman, Tom, Scheres, Ben, Willemsen, Viola, Ten Tusscher, Kirsten, Theoretical Biology and Bioinformatics, Sub Theoretical Biology
Přispěvatelé: Theoretical Biology and Bioinformatics, Sub Theoretical Biology
Jazyk: angličtina
Rok vydání: 2021
Předmět:
computational modeling
Periodicity
Arabidopsis
Gene Expression
Plant Developmental Biology
lateral root priming
Biochemistry
Plant Roots
INITIATION
Plant Growth Regulators
Gene Expression Regulation
Plant

Somitogenesis
NETWORK
periodic developmental patterning
root growth dynamics
food and beverages
Phyllotaxis
ARABIDOPSIS
SEGMENTATION CLOCK
Laboratory of Molecular Biology
Signal Transduction
EXPRESSION
oscillatory priming dynamics
Meristem
CELL-DIVISION
Biology
Models
Biological

General Biochemistry
Genetics and Molecular Biology

experimental validation
Laboratorium voor Moleculaire Biologie
Molecular Biology
Body Patterning
Indoleacetic Acids
Mechanism (biology)
Biochemistry
Genetics and Molecular Biology(all)

Arabidopsis Proteins
Lateral root
Root meristem growth
auxin transport
Biology and Life Sciences
Computational Biology
BASAL MERISTEM
Cell Biology
SELF-ORGANIZATION
plant root branching
GENE
Multicellular organism
Biophysics
Lateral root branching
EPS
Developmental biology
Genetics and Molecular Biology(all)
Developmental Biology
Zdroj: Developmental Cell, 56(15), 2176-2191.e10
Developmental Cell 56 (2021) 15
DEVELOPMENTAL CELL
Developmental Cell, 56(15), 2176. Cell Press
ISSN: 1534-5807
1878-1551
Popis: Modular, repetitive structures are a key component of complex multicellular body plans across the tree of life. Typically, these structures are prepatterned by temporal oscillations in gene expression or signaling. Although a clock-and-wavefront mechanism was identified and plant leaf phyllotaxis arises from a Turing-type patterning for vertebrate somitogenesis and arthropod segmentation, the mechanism underlying lateral root patterning has remained elusive. To resolve this enigma, we combined computational modeling with in planta experiments. Intriguingly, auxin oscillations automatically emerge in our model from the interplay between a reflux-loop-generated auxin loading zone and stem-cell-driven growth dynamics generating periodic cell-size variations. In contrast to the clock-and-wavefront mechanism and Turing patterning, the uncovered mechanism predicts both frequency and spacing of lateral-root-forming sites to positively correlate with root meristem growth. We validate this prediction experimentally. Combined, our model and experimental results support that a reflux-and-growth patterning mechanism underlies lateral root priming.
Databáze: OpenAIRE