Evidence map›Paper›PMID 34256748›Full record

ArticleBMC biology2021

Disruption of left-right axis specification in Ciona induces molecular, cellular, and functional defects in asymmetric brain structures.

Matthew J Kourakis, Michaela Bostwick, Amanda Zabriskie, William C Smith

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 42 citations in OpenAlex.

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  12. Transitions of motor neuron activities duringFrontiers in cell and developmental biology · 2023
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  15. Fold Change Detection in Visual Processing.Frontiers in neural circuits · 2021
    Article
  16. Bilaterally Asymmetric Helical Myofibrils in Ascidian Tadpole Larvae.Frontiers in cell and developmental biology · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Matthew J KourakisNeuroscience Research Institute, University of California, Santa Barbara, CA, 93106, USA.
Michaela BostwickCollege of Creative Studies, University of California, Santa Barbara, CA, 93106, USA.
Amanda ZabriskieDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Barbara, CA, 93106, USA.
William C SmithNeuroscience Research Institute, University of California, Santa Barbara, CA, 93106, USA. w_smith@ucsb.edu.ORCID 0000-0002-6257-7695
University of California, Santa Barbara · US

Funding

Mutational Analysis of Tunicate DevelopmentR01HD038701 · NICHD · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SMITH, WILLIAM · 2000 to 2020
$5.8M
The connectome and neurobiology of a novel model chordate, Ciona intestinalisR01NS103774 · NINDS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI MANJUNATH, BANGALORE S, SMITH, WILLIAM · 2017 to 2021
$2.8M
NICHD NIH HHS R01 HD038701NINDS NIH HHS R01 NS103774
6 · The paper itself

Abstract

backgroundLeft-right asymmetries are a common feature of metazoans and can be found in a number of organs including the nervous system. These asymmetries are particularly pronounced in the simple central nervous system (CNS) of the swimming tadpole larva of the tunicate Ciona, which displays a chordate ground plan. While common pathway elements for specifying the left/right axis are found among chordates, particularly a requirement for Nodal signaling, Ciona differs temporally from its vertebrate cousins by specifying its axis at the neurula stage, rather than at gastrula. Additionally, Ciona and other ascidians require an intact chorionic membrane for proper left-right specification. Whether such differences underlie distinct specification mechanisms between tunicates and vertebrates will require broad understanding of their influence on CNS formation. Here, we explore the consequences of disrupting left-right axis specification on Ciona larval CNS cellular anatomy, gene expression, synaptic connectivity, and behavior.

resultsWe show that left-right asymmetry disruptions caused by removal of the chorion (dechorionation) are highly variable and present throughout the Ciona larval nervous system. While previous studies have documented disruptions to the conspicuously asymmetric sensory systems in the anterior brain vesicle, we document asymmetries in seemingly symmetric structures such as the posterior brain vesicle and motor ganglion. Moreover, defects caused by dechorionation include misplaced or absent neuron classes, loss of asymmetric gene expression, aberrant synaptic projections, and abnormal behaviors. In the motor ganglion, a brain structure that has been equated with the vertebrate hindbrain, we find that despite the apparent left-right symmetric distribution of interneurons and motor neurons, AMPA receptors are expressed exclusively on the left side, which equates with asymmetric swimming behaviors. We also find that within a population of dechorionated larvae, there is a small percentage with apparently normal left-right specification and approximately equal population with inverted (mirror-image) asymmetry. We present a method based on a behavioral assay for isolating these larvae. When these two classes of larvae (normal and inverted) are assessed in a light dimming assay, they display mirror-image behaviors, with normal larvae responding with counterclockwise swims, while inverted larvae respond with clockwise swims.

conclusionsOur findings highlight the importance of left-right specification pathways not only for proper CNS anatomy, but also for correct synaptic connectivity and behavior.

Indexed as

CionaAnimalsBrainCentral Nervous SystemLarvaNeuronsVertebratesAMPA receptorCionaLeft-right asymmetryVisuomotor behavior

Identifiers

PMID34256748
PMCPMC8276506
OpenAlexW3179401312

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.