Evidence map›Paper›PMID 31189599›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

BMP controls dorsoventral and neural patterning in indirect-developing hemichordates providing insight into a possible origin of chordates.

Yi-Hsien Su, Yi-Chih Chen, Hsiu-Chi Ting, Tzu-Pei Fan, Ching-Yi Lin, Kuang-Tse Wang, Jr-Kai Yu

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Early nervous system development in the chaetognathFrontiers in cell and developmental biology · 2026
    Article
  4. Article
  5. Deep homology of aScience advances · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. BMP Signaling: Lighting up the Way for Embryonic Dorsoventral Patterning.Frontiers in cell and developmental biology · 2021
    Review
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

7 authors at 1 institution in 1 country.

Yi-Hsien SuInstitute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan; yhsu@gate.sinica.edu.tw jkyu@gate.sinica.edu.tw.ORCID 0000-0001-6798-9632
Yi-Chih ChenInstitute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan.
Hsiu-Chi TingInstitute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan.
Tzu-Pei FanInstitute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan.
Ching-Yi LinInstitute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan.
Kuang-Tse WangInstitute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan.
Jr-Kai YuInstitute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan; yhsu@gate.sinica.edu.tw jkyu@gate.sinica.edu.tw.ORCID 0000-0001-8591-0529
Institute of Cellular and Organismic Biology, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A defining feature of chordates is the unique presence of a dorsal hollow neural tube that forms by internalization of the ectodermal neural plate specified via inhibition of BMP signaling during gastrulation. While BMP controls dorsoventral (DV) patterning across diverse bilaterians, the BMP-active side is ventral in chordates and dorsal in many other bilaterians. How this phylum-specific DV inversion occurs and whether it is coupled to the emergence of the dorsal neural plate are unknown. Here we explore these questions by investigating an indirect-developing enteropneust from the hemichordate phylum, which together with echinoderms form a sister group of the chordates. We found that in the hemichordate larva, BMP signaling is required for DV patterning and is sufficient to repress neurogenesis. We also found that transient overactivation of BMP signaling during gastrulation concomitantly blocked mouth formation and centralized the nervous system to the ventral ectoderm in both hemichordate and sea urchin larvae. Moreover, this mouthless, neurogenic ventral ectoderm displayed a medial-to-lateral organization similar to that of the chordate neural plate. Thus, indirect-developing deuterostomes use BMP signaling in DV and neural patterning, and an elevated BMP level during gastrulation drives pronounced morphological changes reminiscent of a DV inversion. These findings provide a mechanistic basis to support the hypothesis that an inverse chordate body plan emerged from an indirect-developing ancestor by tinkering with BMP signaling.

Indexed as

Biological EvolutionAnimalsBody PatterningBone Morphogenetic ProteinsChordata, NonvertebrateEmbryo, NonmammalianGastrulationGene Expression Regulation, DevelopmentalLarvaNervous SystemPhylogenySea UrchinsBone Morphogenetic ProteinsBMPchordate originsdorsoventral patterningindirect-developing hemichordatesneural patterning

Identifiers

PMID31189599
PMCPMC6600983
OpenAlexW2951895684

What OpenQuestion holds

Textmetadata
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.