Evidence map›Paper›PMID 41008011›Full record

ArticleAnimals : an open access journal from MDPI2025

A New Family-Based Approach for Detecting Allele-Specific Expression and for Mapping Possible eQTLs.

Maher Alnajjar, Zsófia Fekete, Tibor Nagy, Zoltán Német, Agshin Sakif, Nóra Ninausz, Péter Fehér, Viktor Stéger, Endre Barta

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Maher AlnajjarDepartment of Genetics and Genomics, Institute of Genetics and Biotechnology, Hungarian University of Agriculture and Life Sciences, Szent-Györgyi A. u. 4, H-2100 Gödöllő, Hungary.ORCID 0000-0003-3613-3510
Zsófia FeketeDepartment of Environmental and Biological Sciences, University of Eastern Finland, Yliopistokatu 2, 80100 Joensuu, Finland.ORCID 0000-0002-9086-5459
Tibor NagyDepartment of Genetics and Genomics, Institute of Genetics and Biotechnology, Hungarian University of Agriculture and Life Sciences, Szent-Györgyi A. u. 4, H-2100 Gödöllő, Hungary.ORCID 0000-0002-4451-0796
Zoltán NémetDepartment of Pathology, University of Veterinary Medicine, István u. 2, H-1078 Budapest, Hungary.ORCID 0000-0002-2044-1554
Agshin SakifDepartment of Genetics and Genomics, Institute of Genetics and Biotechnology, Hungarian University of Agriculture and Life Sciences, Szent-Györgyi A. u. 4, H-2100 Gödöllő, Hungary.
Nóra NinauszDepartment of Genetics and Genomics, Institute of Genetics and Biotechnology, Hungarian University of Agriculture and Life Sciences, Szent-Györgyi A. u. 4, H-2100 Gödöllő, Hungary.
Péter FehérDepartment of Genetics and Genomics, Institute of Genetics and Biotechnology, Hungarian University of Agriculture and Life Sciences, Szent-Györgyi A. u. 4, H-2100 Gödöllő, Hungary.
Viktor StégerDepartment of Genetics and Genomics, Institute of Genetics and Biotechnology, Hungarian University of Agriculture and Life Sciences, Szent-Györgyi A. u. 4, H-2100 Gödöllő, Hungary.
Endre BartaDepartment of Genetics and Genomics, Institute of Genetics and Biotechnology, Hungarian University of Agriculture and Life Sciences, Szent-Györgyi A. u. 4, H-2100 Gödöllő, Hungary.ORCID 0000-0002-6753-0714

Funding

Ministry of Culture and Innovation of Hungary from the National Research, Development, and Innovation Fund TKP2021-NKTANational Research, Development and Innovation Office NKFI/2017-1.3.1-VKE-2017-00026National Research, Development and Innovation Office NKFI/OTKA K 132814
6 · The paper itself

Abstract

Allele-specific expression (ASE) reflects the unequal expression of the parental alleles and can imply functional variants in cis-regulatory elements. The conventional ASE detection methods often depend on the presence of heterozygous variants in transcripts or sequencing a large number of individuals, both of which are often limited. In this study, we present a family-based strategy for detecting ASE and potential cis-regulatory elements utilizing both RNA-seq and whole-genome sequencing (WGS) from a pedigree. Using a rabbit family consisting of two divergent parents and their eight offspring, we identified 913 ASE genes by analyzing inheritance patterns of gene expression levels. Expression was classified into three levels-high, medium, and low-and used to define seven distinct expression groups across the family (e.g., H_L: high in the mother, low in the father, and intermediate in the offspring). Many ASE genes lacked heterozygous exonic variants, and inference was achieved via RNA read count patterns. We also pinpointed conserved transcription factor binding sites (TFBS) with sequence variants showing similar inherited genotypic patterns (e.g., AAxBB), suggesting their regulatory roles as eQTLs. Differential gene expression (DEG) analysis between the parents highlighted some candidate genes related to meat production and quality traits. Our findings show that the family-based method using RNA-seq and WGS data is promising for exploring ASE and mapping possible eQTLs.

Indexed as

allele-specific expressioncis-regulatory elementsmeatrabbittranscription factor binding sites

Identifiers

PMID41008011
PMCPMC12466419

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Registered trials

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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.