The origin of animals represents one of the pivotal transitions in life’s history, and one of its greatest unsolved mysteries. While the fossil record remains silent regarding the rise of multicellularity, the genetic and developmental foundations of animal origins may be deduced from shared elements among extant animals and their protozoan relatives, the choanoflagellates. To better understand the origin and evolution of animals, we are:
- reconstructing the minimal genomic complexity of the unicellular progenitors of animals
- elucidating the ancestral functions of genes required for animal development
- characterizing choanoflagellate cell and developmental biology
Cell biology and colony development in choanoflagellates:
The mechanisms by which choanoflagellates form colonies, establish cell polarity, and reproduce may provide crucial insights into the transition to multicellularity, but little is known about their cell biology or natural history. We have recently discovered that there is an unexpected amount of cell differentiation during the life history of the choanoflagellate Salpingoeca rosetta, including the formation of at least two different multicellular colonial forms. These colonies form through a process of incomplete cytokinesis (rather than cell aggregation) such that the mature colony is a clonal individual. In addition, neighboring cells in colonies are linked through fine intercellular bridges that may permit direct sharing of small molecules. Our next goals are to investigate the genetic determinants of cell differentiation and colony formation, through the use of RNA-Seq approaches and the development of genetic screens.
Interspecies interactions in choanoflagellates: Our studies of the choanoflagellate S. rosetta have revealed that its ability to form rosette-shaped colonies is regulated by a chemical signal synthesized by prey bacteria from the genus Algoriphagus. Given the close evolutionary relationship of choanoflagellates to animals and the experimental tractability of the S. rosetta-Algoriphagus interaction, this pairing holds great potential for revealing fundamental mechanisms linking inter-kingdom signaling to morphogenesis. We have been collaborating with the Clardy lab at Harvard Medical School to isolate and identify the bacterially-produced signaling molecule. In addition, we have developed genetic approaches in Algoriphagus to dissect the necessary biosynthetic pathway. Moving forward, a major goal is to isolate the S. rosetta receptor that allows it to perceive and respond to the Algoriphagus signal
Using comparative genomics to investigate the ancestral animal genome: A key question in the origin of animals concerns how and when the “toolkit” of animal genes was assembled. To test whether genes required for animal development evolved before the origin of animal multicellularity, we have sequenced the genomes of the choanoflagellate Monosiga brevicollis and S. rosetta (in collaboration with the JGI and Broad Institute) and are currently preparing to sequence the transcriptomes of 19 additional cultured choanoflagellates as part of the Moore Foundation/NCGR Marine Microbial Eukaryote Transcriptome project. Genes shared only by choanoflagellates and animals were likely present in their common ancestor and may shed light on the transition to multicellularity. This work has already provided evidence that choanoflagellates express members of diverse protein families (e.g. receptor tyrosine kinases, cadherins, and C-type lectins) required for animal cell signaling and adhesion.
Assaying the ancient functions of genes required for multicellular development: The finding of signaling and adhesion gene homologs (e.g. cadherins, receptor tyrosine kinases, and protooncogenes) in choanoflagellates raises questions about how these genes functioned in the unicellular common ancestor of choanoflagellates and animals, and what role they played in the origin of multicellularity. By focusing on the study of cadherins, we have identified a set of previously unidentified cadherin families that were present in the last common ancestor of animals and their last common ancestor with choanoflagellates (the “urchoanimal”). In addition, we have found that the important regulatory interaction between the transcription factor Max and its binding partner Mad evolved before the origin of animals. Inferences about gene function in diverse choanoflagellates provide an important reference point for studies of gene family evolution in animals.