Evidence map›Paper›PMID 28813459›Full record

ArticlePloS one2017

β2-microglobulin gene duplication in cetartiodactyla remains intact only in pigs and possibly confers selective advantage to the species.

Thong Minh Le, Quy Van Chanh Le, Dung Minh Truong, Hye-Jeong Lee, Min-Kyeung Choi, Hyesun Cho, Hak-Jae Chung, Jin-Hoi Kim, Jeong-Tae Do, Hyuk Song and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. 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
0.7field-weighted citation impact, top 31% 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, 9 citations in OpenAlex.

  1. Article
  2. Journal of fungi (Basel, Switzerland) · 2021
    Article
  3. Article
  4. Article
  5. 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

11 authors at 3 institutions in 1 country.

Thong Minh LeDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Quy Van Chanh LeDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Dung Minh TruongDepartment of Molecular Science and Technology, Ajou University, Suwon, Republic of Korea.
Hye-Jeong LeeDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Min-Kyeung ChoiDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Hyesun ChoDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Hak-Jae ChungAnimal Biotechnology Division, National Institute of Animal Science, Rural Development Administration, Wanju-gun, Jeollabuk-do, Republic of Korea.
Jin-Hoi KimDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Jeong-Tae DoDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Hyuk SongDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.
Chankyu ParkDepartment of Stem Cell and Regenerative Biology, Konkuk University, Hwayang-dong, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-4855-2210
Konkuk University · KRAjou University · KRRural Development Administration · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several β2-microglobulin (B2M) -bound protein complexes undertake key roles in various immune system pathways, including the neonatal Fc receptor (FcRn), cluster of differentiation 1 (CD1) protein, non-classical major histocompatibility complex (MHC), and well-known MHC class I molecules. Therefore, the duplication of B2M may lead to an increase in the biological competence of organisms to the environment. Based on the pig genome assembly SSC10.2, a segmental duplication of ~45.5 kb, encoding the entire B2M protein, was identified in pig chromosome 1. Through experimental validation, we confirmed the functional duplication of the B2M gene with a completely identical coding sequence between two copies in pigs. Considering the importance of B2M in the immune system, we performed the phylogenetic analysis of B2M duplication in ten mammalian species, confirming the presence of B2M duplication in cetartioldactyls, like cattle, sheep, goats, pigs and whales, but non-cetartiodactyl species, like mice, cats, dogs, horses, and humans. The density of long interspersed nuclear element (LINE) at the edges of duplicated blocks (39 to 66%) was found to be 2 to 3-fold higher than the average (20.12%) of the pig genome, suggesting its role in the duplication event. The B2M mRNA expression level in pigs was 12.71 and 7.57 times (2-ΔΔCt values) higher than humans and mice, respectively. However, we were unable to experimentally demonstrate the difference in the level of B2M protein because species specific anti-B2M antibodies are not available. We reported, for the first time, the functional duplication of the B2M gene in animals. The identification of partially remaining duplicated B2M sequences in the genomes of only cetartiodactyls indicates that the event was lineage specific. B2M duplication could be beneficial to the immune system of pigs by increasing the availability of MHC class I light chain protein, B2M, to complex with the proteins encoded by the relatively large number of MHC class I heavy chain genes in pigs. Further studies are necessary to address the biological meaning of increased expression of B2M.

Indexed as

Gene DuplicationSelection, GeneticAnimalsBase Sequencebeta 2-MicroglobulinCell LineDNA, ComplementaryGene ExpressionGenomeGenomicsHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryMammalsMiceRNA, Messengerbeta 2-MicroglobulinDNA, ComplementaryRNA, Messenger

Identifiers

PMID28813459
PMCPMC5558954
OpenAlexW2746562972

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.