Developmental biology of the larvacean Oikopleura dioica: Genome resources, functional screening, and imaging.
Takeshi A OnumaHiroki NishidaPublished in: Development, growth & differentiation (2021)
The larvacean Oikopleura dioica is a cosmopolitan planktonic chordate and is closely related to vertebrates. It is characterized by a tadpole-shaped morphology with notochord flanked by muscle in the tail and brain on the dorsal side, a short life cycle of five days, a compact genome of approximately 56 Mb, a simple and transparent body with a small number of cells (~4000 in functional juveniles), invariant embryonic cell lineages, and fast development that ensures complete morphogenesis and organ formation 10 h after fertilization. With these features, this marine chordate is a promising and advantageous animal model in which genetic manipulation is feasible. In this review, we introduce relevant resources and modern techniques that have been developed: (1) Genome and transcriptomes. Oikopleura dioica has the smallest genome among non-parasitic metazoans. Its genome databases have been generated using three geographically distant O. dioica populations, and several intra-species sequence differences are becoming evident; (2) Functional genetic knockdown techniques. Comprehensive screening of genes is feasible using ovarian microinjection and double-strand DNA-induced gene knockdown; and (3) Live imaging of embryos and larvae. Application of these techniques has uncovered novel aspects of development, including meiotic cell arrest, left-right patterning, epidermal cell patterning, and mouth formation involving the connection of ectoderm and endoderm sheets. Oikopleura dioca has become very useful for developmental and evolutionary studies in chordates.
Keyphrases
- genome wide
- single cell
- dna methylation
- copy number
- cell therapy
- high resolution
- life cycle
- gene expression
- skeletal muscle
- spinal cord injury
- spinal cord
- oxidative stress
- bone marrow
- lymph node
- stem cells
- white matter
- photodynamic therapy
- mesenchymal stem cells
- cell proliferation
- signaling pathway
- drug induced
- diabetic rats
- big data
- cell free
- fluorescence imaging
- artificial intelligence
- resting state
- drosophila melanogaster
- cerebral ischemia