Evidence map›Paper›PMID 34379287›Full record

ArticleMolecular biology reports2021

Identification of sequence variation in the oocyte-derived bone morphogenetic protein 15 (BMP15) gene (BMP15) associated with litter size in New Zealand sheep (Ovis aries) breeds.

Hamed Amirpour Najafabadi, Majid Khansefid, Ghassan Ghaith Mahmoud, Ishaku Lemu Haruna, Huitong Zhou, Jon G H Hickford

Abstract read
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In one paragraph

Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

5 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Association ofGenes · 2025
    Article
  3. Article
  4. Effects of New Mutations inVeterinary sciences · 2023
    Article
  5. Detection of Novel Variations Related to Litter Size inAnimals : an open access journal from MDPI · 2021
    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

6 authors at 2 institutions in 2 countries.

Hamed Amirpour NajafabadiGene-Marker Laboratory, Department of Agricultural Sciences, Lincoln University, Lincoln, 7647, Christchurch, New Zealand.
Majid KhansefidAgriculture Victoria, AgriBio, Centre for AgriBioscience, Bundoora, VIC, 3083, Australia.
Ghassan Ghaith MahmoudGene-Marker Laboratory, Department of Agricultural Sciences, Lincoln University, Lincoln, 7647, Christchurch, New Zealand.
Ishaku Lemu HarunaGene-Marker Laboratory, Department of Agricultural Sciences, Lincoln University, Lincoln, 7647, Christchurch, New Zealand.
Huitong ZhouGene-Marker Laboratory, Department of Agricultural Sciences, Lincoln University, Lincoln, 7647, Christchurch, New Zealand.
Jon G H HickfordGene-Marker Laboratory, Department of Agricultural Sciences, Lincoln University, Lincoln, 7647, Christchurch, New Zealand. Jonathan.Hickford@lincoln.ac.nz.ORCID http://orcid.org/0000-0001-9313-761X
Lincoln University · NZAgriculture Victoria · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in the study of reproductive traits indicate that functional variation in fertility genes may be useful for improving sheep fertility. The aim of this study was to search for variation in the bone morphogenetic protein 15 gene (BMP15) and ascertain any association with litter size in purebred Finnish Landrace sheep (n = 148), Finnish Landrace × Texel-cross sheep (n = 45), and composite sheep (of varying breed background; n = 58) from New Zealand (NZ). A 482 bp and 312 bp fragment of exon 1 and 2, respectively, of BMP15 were analysed using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP). The additive and dominance effect of BMP15 variation on litter size were estimated using animal and sire models. Two variants (A and B) were detected in exon 1; no sequence variation was detected in exon 2. Variant A had the nucleotide sequence CTT between positions c.31 and c.33, while variant B had a deletion (c.31_33del). The observed frequency for variant A in the Finnish Landrace sheep, Finnish Landrace × Texel-cross sheep and the composite sheep, was 0.77, 0.92, and 0.68, respectively while the frequency of variant B (c.31_33del) was 0.23, 0.08, and 0.32, respectively. An association between litter size and c.31_33del (P < 0.001) was observed in composite sheep. Analysis of more sheep will be required to confirm these results. Litter size did not differ significantly between sheep breeds regardless of the presence/absence of c.31_33del. Results suggested that c.31_33del might be a genetic marker for improving fecundity in some NZ sheep.

Indexed as

AllelesPolymorphism, GeneticAnimalsBase SequenceBone Morphogenetic Protein 15ExonsFemaleFertilityHeterozygoteHomozygoteLitter SizeMutationNew ZealandOocytesPolymerase Chain ReactionPregnancyBone Morphogenetic Protein 15Bone morphogenic protein 15 geneLitter sizeNew Zealand (NZ)Ovis ariesSheep

Identifiers

PMID34379287
OpenAlexW3193073938

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.