Evidence map›Paper›PMID 34599683›Full record

ArticleMolecular genetics and genomics : MGG2021

A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle.

Joana G P Jacinto, Irene M Häfliger, Inês M B Veiga, Anna Letko, Arcangelo Gentile, Cord Drögemüller

Open access · hybridAbstract read
In one paragraph

Article in Molecular genetics and genomics : MGG, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 30% of its field
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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Genome-wide detection of copy number variations in indigenous Red Sindhi cattle using ddRAD sequencing.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Article
  3. Article
  4. Review
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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

6 authors at 2 institutions in 2 countries.

Joana G P JacintoDepartment of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, 40064, Bologna, Italy.ORCID http://orcid.org/0000-0002-6438-7975
Irene M HäfligerInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.ORCID http://orcid.org/0000-0002-5648-963X
Inês M B VeigaInstitute of Animal Pathology, Vetsuisse Faculty, University of Bern, 3012, Bern, Switzerland.ORCID http://orcid.org/0000-0001-8554-790X
Anna LetkoInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.ORCID http://orcid.org/0000-0002-6521-1285
Arcangelo GentileDepartment of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia, 40064, Bologna, Italy.ORCID http://orcid.org/0000-0002-6091-8978
Cord DrögemüllerInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland. cord.droegemueller@vetsuisse.unibe.ch.ORCID http://orcid.org/0000-0001-9773-522X
University of Bern · CHUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to characterize the phenotype and to identify the genetic etiology of a syndromic form of ichthyosis congenita (IC) observed in Italian Chianina cattle and to estimate the prevalence of the deleterious allele in the population. Sporadic occurrence of different forms of ichthyosis including IC have been previously reported in cattle. However, so far, no causative genetic variant has been found for bovine IC. Nine affected cattle presenting congenital xerosis, hyperkeratosis and scaling of the skin as well as urolithiasis and cystitis associated with retarded growth were examined. Skin histopathology revealed a severe, diffuse orthokeratotic hyperkeratosis with mild to moderate epidermal hyperplasia. The pedigree records indicated a monogenic recessive trait. Homozygosity mapping and whole-genome sequencing allowed the identification of a homozygous frameshift 1 bp insertion in the FA2H gene (c.9dupC; p.Ala4ArgfsTer142) located in a 1.92 Mb shared identical-by-descent region on chromosome 18 present in all cases, while the parents were heterozygous as expected for obligate carriers. These findings enable the selection against this sub-lethal allele showing an estimated frequency of ~ 7.5% in Chianina top sires. A sporadic incidence of mild clinical signs in the skin of heterozygous carriers was observed. So far, pathogenic variants affecting the encoded fatty acid 2-hydroxylase catalyzing the synthesis of 2-hydroxysphingolipids have been associated with myelin disorders. In conclusion, this study represents the first report of an FA2H-related autosomal recessive inherited skin disorder in a mammalian species and adds FA2H to the list of candidate genes for ichthyosis in humans and animals. Furthermore, this study provides a DNA-based diagnostic test that enables selection against the identified pathogenic variant in the Chianina cattle population. However, functional studies are needed to better understand the expression of FA2H in IC-affected Chianina cattle.

Indexed as

AnimalsCattleCattle DiseasesFrameshift MutationGenetic Predisposition to DiseaseGenomeIchthyosis, LamellarMixed Function OxygenasesSkinSphingolipidsWhole Genome SequencingMixed Function OxygenasesSphingolipidsBovineFatty acid 2-hydroxylaseGenodermatosesPrecision medicineSkinUrolithiasis

Identifiers

PMID34599683
PMCPMC8550120
OpenAlexW3203391806

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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.