MétaCan
Menu
Back to cohort

Untangling Sources of Phenotypic Variation Characterizing the Craniofacial Disease Holoprosencephaly

2018· article· en· W3173614491 on OpenAlexaff
Alexis Lainoff, Nathan M. Young, Benedikt Hallgrímsson, Ralph Marcucio

Bibliographic record

VenueThe FASEB Journal · 2018
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicHedgehog Signaling Pathway Studies
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsHoloprosencephalySonic hedgehogCraniofacialForebrainPhenotypeBiologyCyclopiaAlleleGeneticsEndocrinologyInternal medicineSignal transductionMedicineGeneFetusCentral nervous system

Abstract

fetched live from OpenAlex

Holoprosencaphly (HPE)—a craniofacial disorder in which the forebrain fails to develop into two hemispheres and the midface does not fully form—is characterized by a broad spectrum of severity. Phenotypes range from very mild midfacial narrowing to cyclopia. Mutations in Sonic hedgehog (SHH) and in SHH signaling pathway members are known to underlie HPE; however, the source of the highly variable craniofacial morphology manifesting in the HPE patient population is not understood. Previous research in a chick model suggests that reduced SHH‐signaling in the brain correlates with a continuous distribution of HPE‐like phenotypes, and that very small modifications in ligand concentration can result in highly heterogeneous morphologies. Here, we are probing the origins of morphological variation in a genetic mouse model. Although humans heterozygous for SHH mutations exhibit the full spectrum of HPE, mice heterozygous for Shh do not exhibit even mild HPE although homozygous mutants are cyclopic. Mice homozygous for mutations in the SHH‐signaling pathway member low‐density lipoprotein receptor‐related protein (Lrp) 2 however exhibit mild to severe forms of HPE, and are therefore a better model for examining sources of variation. LRP2 is an endocytic receptor required to induce proper SHH signaling in the forebrain. We used geometric morphometric analysis to quantify the shape of embryos with sequential, genetic loss of Shh and Lrp2 alleles, and qPCR was used to assess SHH signaling pathway activation. We found that there is no statistically significant difference in shape among wild‐type, Lrp2+/− , Shh+/− , and Lrp2+/−;Shh+/− embryos, while Lrp2−/− and Lrp2−/−;Shh+/− embryos diverged from the group, exhibiting a more narrow midface. Interestingly, there was increased phenotypic variance in Lrp2−/− and Lrp2−/−;Shh+/− embryos in comparison to the other genotypes, with a greater increase in variance seen in the Lrp2−/−;Shh+/− group. Our results support the hypothesis that very slight modifications to SHH pathway activation can yield large amounts of phenotypic variation. Support or Funding Information This work is supported by NIH/NIDCR‐R01DE018234, ‐R01DE019638, ‐T32DE730619, ‐F31DE02579001. This abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal .

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0000.001
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.016
GPT teacher head0.244
Teacher spread0.228 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2018
Admission routes1
Has abstractyes

Explore more

Same venueThe FASEB JournalSame topicHedgehog Signaling Pathway StudiesFrench-language works237,207