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Cell Size and Flexible Cell Fate Decisions in the Stomatal Lineage.
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Cell Size and Flexible Cell Fate Decisions in the Stomatal Lineage.
자료유형  
 학위논문
Control Number  
0017162939
International Standard Book Number  
9798384337362
Dewey Decimal Classification Number  
612
Main Entry-Personal Name  
Fung, Hannah F.
Publication, Distribution, etc. (Imprint  
[S.l.] : Stanford University., 2024
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2024
Physical Description  
148 p.
General Note  
Source: Dissertations Abstracts International, Volume: 86-03, Section: B.
General Note  
Advisor: Bergmann, Dominique;Dinneny, Jose;Red-Horse, Kristy;Wang, Bo.
Dissertation Note  
Thesis (Ph.D.)--Stanford University, 2024.
Summary, Etc.  
요약In plants, stomata are epidermal valves through which carbon dioxide enters and oxygen and water escape. Collectively, stomata are major players in global carbon and water cycles, regulating wateruse efficiency across entire ecosystems. In tropical forests, an estimated 32 x 1015 kilograms of water vapour pass through stomata each year, which is more than double the water vapour cycling through the atmosphere annually (15 x 1015 kg per year; Hetherington and Woodward, 2003).In dicots, stomata comprise a pair of guard cells flanking a central pore. The size of this pore defines the stomatal conductance or the rate at which gases diffuse through the pore. While stomatal conductance varies with environmental conditions, the maximum stomatal conductance is developmentally constrained. This theoretical maximum increases with stomatal number, which is specified during development. To modulate the physiological potential of a leaf, we need to understand how developmental events regulate stomatal number.There are two common measures of stomatal number: stomatal density (the number of stomata per millimeter ) and stomatal index (the proportion of leaf epidermal cells that are stomata). There are several reasons why stomatal index is more informative from a developmental perspective. First, unlike stomatal density, which generally increases from leaf base to tip, stomatal index shows little intra-leaf variation. Second, stomatal index is independent of cell size and is therefore robust to factors that influence cell expansion independently of stomatal number. Finally, stomatal index is a measure of cell type composition, which reflects the division and differentiation events that took place to build the organ.In many species, stomatal index is flexible, increasing with light intensity and decreasing with osmotic stress. Similarly, both short- and long-term studies point to an inverse relationship between carbon dioxide levels and stomatal index. Higher stomatal indices are expected to increase carbon assimilation rates, but at the cost of increased transpiration. What cellular behaviours underlie this developmental flexibility?In this dissertation, I address this question using the model organism, Arabidopsis thaliana,where the stomatal lineage produces the majority of leaf epidermal cells. This lineage begins when a subset of protodermal cells is stochastically selected to become meristemoid mother cells, which divide asymmetrically to produce two daughter cells. The smaller daughter, or the meristemoid, can either differentiate into a stoma or undergo one or more asymmetric divisions before differentiating. The larger daughter, or the stomatal lineage ground cell (SLGC), faces a similar choice: it can either differentiate into a cuticle-producing pavement cell or divide to generate another meristemoid and SLGC.Generally, the stomatal index remains constant when cells differentiate directly. It tends to decrease when meristemoids divide and increase when SLGCs divide. Consequently, the cell type composition of a leaf is regulated by the frequency at which meristemoids and SLGCs divide. In this dissertation, I identify and characterize factors that regulate the frequency of asymmetric cell divisions in the stomatal lineage. I show that cell size influences both meristemoid and SLGC behaviours, but in surprisingly different ways.
Subject Added Entry-Topical Term  
Physiology.
Subject Added Entry-Topical Term  
Embryos.
Subject Added Entry-Topical Term  
Behavior.
Subject Added Entry-Topical Term  
Homeostasis.
Subject Added Entry-Topical Term  
Severe acute respiratory syndrome coronavirus 2.
Subject Added Entry-Topical Term  
Insects.
Subject Added Entry-Topical Term  
Genomes.
Subject Added Entry-Topical Term  
Age groups.
Subject Added Entry-Topical Term  
Biology.
Subject Added Entry-Topical Term  
Metabolism.
Subject Added Entry-Topical Term  
Phosphorylation.
Subject Added Entry-Topical Term  
Apoptosis.
Subject Added Entry-Topical Term  
Stem cells.
Subject Added Entry-Topical Term  
Households.
Subject Added Entry-Topical Term  
Cell cycle.
Subject Added Entry-Topical Term  
Transcription factors.
Subject Added Entry-Topical Term  
Disease transmission.
Subject Added Entry-Topical Term  
Cellular biology.
Subject Added Entry-Topical Term  
Genetics.
Added Entry-Corporate Name  
Stanford University.
Host Item Entry  
Dissertations Abstracts International. 86-03B.
Electronic Location and Access  
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Control Number  
joongbu:657428
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