Dissecting the cellular and molecular basis of photosymbiosis in the acoel convolutriloba longifissura

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Abstract/Contents

Abstract
Multicellular organisms are now commonly regarded as holobionts, collections of species making up an individual. The intimate relationships between symbiotes in a holobiont seem to involve the molecular interdependence of species to varying degrees. Studying the integration of molecular pathways in holobionts has been experimentally challenging, but high-throughput sequencing technologies now allow for the simultaneous evaluation of multiple partners at once. In this dissertation, we use the photosymbiotic acoel Convolutriloba longifissura to evaluate some of the implications of the molecular crosstalk between species. In Chapter 2, we evaluate the responses of algal symbionts to host regeneration. Early post-injury the algal response is defined by a decrease in photosynthetic efficiency and an upregulation of photosynthesis-related genes. A second wave of transcriptional responses takes place two days post-injury, with unique molecular players. We demonstrate that regeneration of the holobiont is dependent on the transcription factor, Cl-runt, a conserved regulator of acoel regeneration. Knockdown of Cl-runt further decreases the operational quantum yield of photosystem II and dampens the early and late transcriptional responses in both the host and the symbionts. This work describes the coordination of molecular responses to regeneration in a photosymbiotic holobiont. In Chapter 3 we characterize the cell type diversity found in C. longifissura and compare their cell type composition to the non-symbiotic acoel Hofstenia miamia. We identify 17 unique cell types belonging to all expected tissue types: epidermal, muscle, neural, endoderm-like, secretory, and stem cells. Based on their relative DNA content and gene expression, four populations are cycling stem cells. Comparison with H. miamia demonstrates high cell type similarity. Muscle and epidermal cell types have the best alignment scores, while stem cells share the highest number of supporting genes. The endoderm-like cell types are identified as homologs but show low similarity. However, we identify five orthologous transcription factors shared between acoel endoderm-like cell types: foxA, ets-2, gsc, hnf4, and elf5. Functional characterization is needed to evaluate if these cell types have shared functions in these acoels. Overall, the high similarity found between acoel cell types supports a limited cell type divergence between acoels.

Description

Type of resource text
Form electronic resource; remote; computer; online resource
Extent 1 online resource.
Place California
Place [Stanford, California]
Publisher [Stanford University]
Copyright date 2024; ©2024
Publication date 2024; 2024
Issuance monographic
Language English

Creators/Contributors

Author Nanes Sarfati, Dania
Degree supervisor Wang, Bo, (Researcher in bioengineering)
Thesis advisor Wang, Bo, (Researcher in bioengineering)
Thesis advisor Bergmann, Dominique
Thesis advisor Lowe, Christopher, (Associate professor of biology)
Thesis advisor Palumbi, Stephen R
Degree committee member Bergmann, Dominique
Degree committee member Lowe, Christopher, (Associate professor of biology)
Degree committee member Palumbi, Stephen R
Associated with Stanford University, School of Humanities and Sciences
Associated with Stanford University, Department of Biology

Subjects

Genre Theses
Genre Text

Bibliographic information

Statement of responsibility Dania Nanes Sarfati.
Note Submitted to the Department of Biology.
Thesis Thesis Ph.D. Stanford University 2024.
Location https://purl.stanford.edu/nn462jb7266

Access conditions

Copyright
© 2024 by Dania Nanes Sarfati
License
This work is licensed under a Creative Commons Attribution 3.0 Unported license (CC BY).

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