Evidence map›Paper›PMID 39506635›Full record

ArticleBMC genomics2024

Molecular cloning of PRD-like homeobox genes expressed in bovine oocytes and early IVF embryos.

Barış Yaşar, Nina Boskovic, Marilin Ivask, Jere Weltner, Eeva-Mari Jouhilahti, Piibe Vill, Tiina Skoog, Ülle Jaakma, Juha Kere, Thomas R Bürglin and 3 more

Abstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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

13 authors.

Barış YaşarDepartment of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia. baris.yasar@ut.ee.
Nina BoskovicDepartment of Medicine Huddinge, Karolinska Institutet, Huddinge, Sweden.
Marilin IvaskChair of Animal Breeding and Biotechnology, Institute of Veterinary Medicine and Animal Sciences, Estonian University of Life Sciences, Tartu, Estonia.
Jere WeltnerFolkhälsan Research Centre, Helsinki, Finland.
Eeva-Mari JouhilahtiFolkhälsan Research Centre, Helsinki, Finland.
Piibe VillDepartment of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Tiina SkoogDepartment of Medicine Huddinge, Karolinska Institutet, Huddinge, Sweden.
Ülle JaakmaChair of Animal Breeding and Biotechnology, Institute of Veterinary Medicine and Animal Sciences, Estonian University of Life Sciences, Tartu, Estonia.
Juha KereDepartment of Medicine Huddinge, Karolinska Institutet, Huddinge, Sweden.
Thomas R BürglinDepartment of Biomedicine, University of Basel, Basel, Switzerland.
Shintaro KatayamaDepartment of Medicine Huddinge, Karolinska Institutet, Huddinge, Sweden.
Tõnis OrgDepartment of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Ants KurgDepartment of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEmbryonic genome activation (EGA) is a critical step in early embryonic development, as it marks the transition from relying on maternal factors to the initiation of transcription from embryo's own genome. The factors associated with EGA are not well understood and need further investigation. PRD-like (PRDL) homeodomain transcription factors (TFs) are considered to play crucial roles in this early event during development but these TFs have evolved differently, even within mammalian lineages. Different numbers of PRDL TFs have been predicted in bovine (Bos taurus); however, their divergent evolution requires species-specific confirmation and functional investigations.

resultsIn this study, we conducted molecular cloning of mRNAs for the PRDL TFs ARGFX, DUXA, LEUTX, NOBOX, TPRX1, TPRX2, and TPRX3 in bovine oocytes or in vitro fertilized (IVF) preimplantation embryos. Our results confirmed the expression of PRDL TF genes in early bovine development at the cDNA level and uncovered their structures. For each investigated PRDL TF gene, we isolated at least one homeodomain-encoding cDNA fragment, indicative of DNA binding and thus potential role in transcriptional regulation in developing bovine embryos. Additionally, our cDNA cloning approach allowed us to reveal breed-related differences in bovine, as evidenced by the identification of a high number of single nucleotide variants (SNVs) across the PRDL class homeobox genes. Subsequently, we observed the prediction of the 9aa transactivation domain (9aaTAD) motif in the putative protein sequence of TPRX3 leading us to conduct functional analysis of this gene. We demonstrated that the TPRX3 overexpression in bovine fibroblast induces not only protein-coding genes but also short noncoding RNAs involved in splicing and RNA editing. We supported this finding by identifying a shared set of genes between our and published bovine early embryo development datasets.

conclusionsProviding full-length cDNA evidence for previously predicted homeobox genes that belong to PRDL class improves the annotation of the bovine genome. Updating the annotation with seven developmentally-important genes will enhance the accuracy of RNAseq analysis with datasets derived from bovine preimplantation embryos. In addition, the absence of TPRX3 in humans highlights the species-specific and TF-specific regulation of biological processes during early embryo development.

Indexed as

Cloning, MolecularFertilization in VitroGenes, HomeoboxHomeodomain ProteinsOocytesAnimalsBlastocystCattleEmbryonic DevelopmentGene Expression Regulation, DevelopmentalTranscription FactorsHomeodomain ProteinsTranscription FactorsBovineHomeodomainPRD-like (PRDL) domainPreimplantation embryo developmentReproduction

Identifiers

PMID39506635
PMCPMC11542365

What Socratic holds

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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 Socratic graph.