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Record W4319079226 · doi:10.1186/s12915-022-01475-0

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

2023· article· en· W4319079226 on OpenAlexafffund
Justine M. Chee, Louise Lanoue, Dave Clary, Kendall Higgins, Lynette Bower, Ann M. Flenniken, Ruolin Guo, David J. Adams, Fátima Bosch, Robert E. Braun, Steve D. M. Brown, Hyungjin Chin, Mary E. Dickinson, Chih‐Wei Hsu, Michael S. Dobbie, Xiang Gao, Sanjeev Galande, Anne Grobler, Jason D. Heaney, Yann Hérault, Martin Hrabě de Angelis, Fabio Mammano, Lauryl M. J. Nutter, Helen Parkinson, Chuan Qin, Toshi Shiroishi, Radislav Sedláček, Je Kyung Seong, Ying Xu, Cheryl L. Ackert‐Bicknell, Douglas E. Adams, Anne‐Tounsia Adoum, Juan Antonio Aguilar‐Pimentel, Uchechukwu Akoma, Dalila Ali-Hadji, Oana V. Amarie, Philippe André, Aurélie Auburtin, Chaouki Bam’Hamed, Johannes Beckers, Joachim Beig, Zorana Berberovic, Alexandr Bezginov, Marie‐Christine Birling, Katharina Boroviak, Joanna Bottomley, Antje Bürger, Dirk H. Busch, Natalie C. Butterfield, Pilar Cacheiro, Julia Calzada‐Wack, Emma L. Cambridge, Susan Camilleri, Marie‐France Champy, Heather Cater, Philippe Charles, Elissa J. Chesler, Yi-Li Cho, Audrey E. Christiansen, Valentina Cipriani, Nicola Cockle, Gemma Codner, Amie Creighton, Maribelle Cruz, Katharine F. Curry, Abigail D’Souza, Ozge Danisment, Daniel Delbarre, Hannah F. Dewhurst, Brendan Doe, Alex Dorr, Florian Giesert, Graham Duddy, Kyle Duffin, Amal El Amri, Hillary Elrick, Mohammad Eskandarian, Martin Fray, Anthony Frost, Helmut Fuchs, Valérie Gailus‐Durner, Karen Kristine Gampe, Milan Ganguly, David Gannon, Lillian Garrett, Marina Gertsenstein, Diane Gleeson, Leslie O. Goodwin, Jochen Graw, Kristin Grimsrud, Hamed Haselimashhadi, Liane Hobson, Andreas Hörlein, Sabine M. Hölter, Seung-Hyun Hong, Neil Horner, Amanda Trainor, Ziyue Huang, Coleen Kane, Yulia Katsman, Lance C. Keith, Lois Kelsey, Janet Kenyon, Ruairidh King, Piia Keskivali-Bond, Andrea Kirton, Tanja Klein‐Rodewald, Thomas Klopstock, Davide Komla‐Ebri, Tomasz Konopka, Ralf Kühn, Fiona Kussy, David Lafont, Qing Lan, Denise G. Lanza, Valerie Laurin, Elise Le Marchand, Sophie Leblanc, Victoria D. Leitch, Chris Lelliott, Christoph Lengger, Lauri G. Lintott, John G. Logan, Isabel Lorenzo, Ann‐Marie Mallon, Naila S. Mannan, Susan Marschall, Melissa L. McElwee, Matthew Mckay, Robbie S. B. McLaren-Jones, Jeremy Mason, Terrence F. Meehan, D. Craig Miller, Michayla Moore, Violeta Muñoz‐Fuentes, Stephen A. Murray, Dong Nguyen-Bresinsky, Oskar Oritz, Panos Pandis, Alexandru Parlog, Amit Patel, Guillaume Pavlovic, Monica Pereira, Kevin A. Peterson, Vivek M. Philip, Andrea S. Pollard, Jan Procházka, Dawei Qu, Ayexa Ramirez, Sean Rangarajan, Tara L. Rasmussen, Birgit Rathkolb, Mike Relac, Kyle Roberton, Willson Roper, Stéphane Rousseau, David W. Rowe, Jan Rozman, Jennifer Ryan, Edward J. Ryder, Luís Santos, Adrián Sanz‐Moreno, Joel Schick, Zachary Seavey, John R. Seavitt, Claudia Seisenberger, Mohammed Selloum, Xueyuan Shang, Dong‐Guk Shin, Michelle Simon, Gillian Sleep, Damian Smedley, Tania Sorg, Penny C. Sparkes, Nadine Spielmann, Ralph Steinkamp, Michelle Stewart, Claudia Stoeger, Ewan Straiton, Karen L. Svenson, Holly Swash, Lydia Teboul, Sandra Tondat, Irina Treise, Catherine Tudor, Rachel Urban, Valerie E. Vancollie, Laurent Vasseur, Igor Vukobradovic, Hannah Wardle‐Jones, Jonathan Warren, Marie Wattenhofer‐Donzé, Sara E. Wells, Jacqueline K. White, Jean-Paul Wiegand, Amelia Willett, Catherine Witmeyer, Eckhard Wolf, Leeyean Wong, Joshua Wood, Wolfgang Wurst, Catherine K. Xu, Annemarie Zimprich, Brian P. Brooks, Colin McKerlie, K. C. Kent Lloyd, Henrik Westerberg, Ala Moshiri

Bibliographic record

VenueBMC Biology · 2023
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicOcular Disorders and Treatments
Canadian institutionsUniversity of TorontoHospital for Sick ChildrenToronto Centre for PhenogenomicsLunenfeld-Tanenbaum Research Institute
FundersNational Eye InstituteNational Human Genome Research InstituteNational Institutes of HealthMedical Research CouncilGenome Canada
KeywordsEye developmentMicrophthalmiaBiologyAnophthalmiaColobomaGeneticsPAX6Gene knockoutGeneCandidate genePhenotype

Abstract

fetched live from OpenAlex

BACKGROUND: Microphthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of eye malformations which play a role in childhood visual impairment. Although the predominant cause of eye malformations is known to be heritable in nature, with 80% of cases displaying loss-of-function mutations in the ocular developmental genes OTX2 or SOX2, the genetic abnormalities underlying the remaining cases of MAC are incompletely understood. This study intended to identify the novel genes and pathways required for early eye development. Additionally, pathways involved in eye formation during embryogenesis are also incompletely understood. This study aims to identify the novel genes and pathways required for early eye development through systematic forward screening of the mammalian genome. RESULTS: Query of the International Mouse Phenotyping Consortium (IMPC) database (data release 17.0, August 01, 2022) identified 74 unique knockout lines (genes) with genetically associated eye defects in mouse embryos. The vast majority of eye abnormalities were small or absent eyes, findings most relevant to MAC spectrum disease in humans. A literature search showed that 27 of the 74 lines had previously published knockout mouse models, of which only 15 had ocular defects identified in the original publications. These 12 previously published gene knockouts with no reported ocular abnormalities and the 47 unpublished knockouts with ocular abnormalities identified by the IMPC represent 59 genes not previously associated with early eye development in mice. Of these 59, we identified 19 genes with a reported human eye phenotype. Overall, mining of the IMPC data yielded 40 previously unimplicated genes linked to mammalian eye development. Bioinformatic analysis showed that several of the IMPC genes colocalized to several protein anabolic and pluripotency pathways in early eye development. Of note, our analysis suggests that the serine-glycine pathway producing glycine, a mitochondrial one-carbon donator to folate one-carbon metabolism (FOCM), is essential for eye formation. CONCLUSIONS: Using genome-wide phenotype screening of single-gene knockout mouse lines, STRING analysis, and bioinformatic methods, this study identified genes heretofore unassociated with MAC phenotypes providing models to research novel molecular and cellular mechanisms involved in eye development. These findings have the potential to hasten the diagnosis and treatment of this congenital blinding disease.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.064
Threshold uncertainty score0.434

Codex and Gemma teacher scores by category

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

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 head0.019
GPT teacher head0.262
Teacher spread0.243 · 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 teacher head, 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

Citations23
Published2023
Admission routes2
Has abstractyes

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