Kira Treibergs Thesis Defense (Robert Woollacott Lab)

Date: 

Wednesday, May 1, 2019, 10:00am

Location: 

Biological Labs Lecture Hall 1080, 16 Divinity Avenue

Title: How Does A Polymorphic Colony Divide Labor Among Its Modules? Colonial Development in the Marine Invertebrate, Bugulina stolonifera

Abstract: Bryozoans are a diverse phylum of marine and freshwater colonial invertebrates containing approximately 6,000 described living species. Bryozoans grow by budding new physiologically connected colony members (zooids) from a metamorphosed larva. Interestingly, these modules often come in different shapes and sizes and are specialized to serve different tasks within the colony. Zooids range in function from feeding to reproduction, structure, defense, and colony attachment. A complex interaction of genotype, environment, and developmental pathway shapes zooid formation, however, the specific mechanisms underlying the establishment of this division of labor remain unknown.

In this thesis, I present the first characterizations of differential gene expression between polymorphic zooids of a bryozoan colony. I explored the development and morphology of different zooid types of lab-cultured Bugulina stolonifera colonies using RNA sequencing, de novo transcriptome assembly, and differential gene analysis. I developed a technique to extract high quality mRNA from small colony structures (<100 μm avicularia and < 50 μm avicularia buds) which enabled me to build cDNA libraries for three different zooid types at two different developmental stages with three biological replicates per tissue. High throughput sequencing of cDNA libraries on the Illumina platform yielded an average of 20.1 million paired-end reads per sample, from which I filtered all low-quality and potential contaminant sequences, resulting in an average of 14.9 ± 1.3 (SE) million paired-end reads per sample. Here, I present data for the first de novo transcriptome assemblies of B. stolonifera and the first characterization of genes involved in the formation and maintenance of zooid types within a bryozoan colony.

De novo assembly resulted in an average of 250,000 transcripts per sample, with an average N50 contig size of 956 base pairs. In a comparison between autozooid and avicularium tissues, I uncovered 1,097 significant differentially expressed genes and retreived blast hits for 52% of those transcripts against the NCBI non-redundant database and identified gene ontology (GO) terms for 39% of transcripts. To further explore the development of the avicularium from bud to mature state, I used confocal imaging to define four broad morphological stages of avicularian ontogeny and described the defining characteristics of each stage. Taken together, this work provides a much-needed foundation for a new approach to understanding the mechanisms involved in the development of zooids and the establishment of division of labor of B. stolonifera, and contributes new insights into the evolution of polymorphism in bryozoans.

 

Committee: Robert Woollacott (Advisor), Cassandra Extavour, Gonzalo Giribet, David Haig