Evidence map›Paper›PMID 39484405›Full record

ArticlebioRxiv : the preprint server for biology2024

Cellular and molecular mechanisms that shape the development and evolution of tail vertebral proportion in mice and jerboas.

Ceri J Weber, Alexander J Weitzel, Alexander Y Liu, Erica G Gacasan, Robert L Sah, Kimberly L Cooper

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Ceri J WeberDepartment of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.ORCID 0000-0001-7846-2094
Alexander J WeitzelDepartment of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.ORCID 0000-0002-1713-158X
Alexander Y LiuDepartment of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Erica G GacasanShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California, USA.ORCID 0000-0002-3145-7615
Robert L SahShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California, USA.ORCID 0000-0002-5493-9502
Kimberly L CooperDepartment of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.ORCID 0000-0001-5892-8838

Funding

Leveraging comparative genomics to elucidate the genetic determinants of limb skeletal proportionR01AR075415 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI COOPER, KIMBERLY LYNN · 2019 to 2023
$1.9M
Illumina NovaSeq 6000 Sequencing SystemS10OD026929 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEPSEN, KRISTEN LYNN · 2019 to 2019
$600k
Cellular and Genetic Determinants that Establish and Diversify Proportion in the Vertebral SkeletonF32AR079923 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WEBER, CERI · 2021 to 2023
$205k
NIAMS NIH HHS F32 AR079923NIAMS NIH HHS R01 AR075415NIH HHS S10 OD026929
6 · The paper itself

Abstract

Despite the functional importance of the vertebral skeleton, little is known about how individual vertebrae elongate or achieve disproportionate lengths as in the giraffe neck. Rodent tails are an abundantly diverse and more tractable system to understand mechanisms of vertebral growth and proportion. In many rodents, disproportionately long mid-tail vertebrae form a 'crescendo-decrescendo' of lengths in the tail series. In bipedal jerboas, these vertebrae grow exceptionally long such that the adult tail is 1.5x the length of a mouse tail, relative to body length, with four fewer vertebrae. How do vertebrae with the same regional identity elongate differently from their neighbors to establish and diversify adult proportion? Here, we find that vertebral lengths are largely determined by differences in growth cartilage height and the number of cells progressing through endochondral ossification. Hypertrophic chondrocyte size, a major contributor to differential elongation in mammal limb bones, differs only in the longest jerboa mid-tail vertebrae where they are exceptionally large. To uncover candidate molecular mechanisms of disproportionate vertebral growth, we performed intersectional RNA-Seq of mouse and jerboa tail vertebrae with similar and disproportionate elongation rates. Many regulators of posterior axial identity and endochondral elongation are disproportionately differentially expressed in jerboa vertebrae. Among these, the inhibitory natriuretic peptide receptor C (NPR3) appears in multiple studies of rodent and human skeletal proportion suggesting it refines local growth rates broadly in the skeleton and broadly in mammals. Consistent with this hypothesis, NPR3 loss of function mice have abnormal tail and limb proportions. Therefore, in addition to genetic components of the complex process of vertebral evolution, these studies reveal fundamental mechanisms of skeletal growth and proportion.

Identifiers

PMID39484405
PMCPMC11527341

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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.