Evidence map›Paper›PMID 34914745›Full record

ArticlePloS one2021

Lower promoter activity of the ST8SIA2 gene has been favored in evolving human collective brains.

Toshiyuki Hayakawa, Masahiro Terahara, Naoko T Fujito, Takumi Matsunaga, Kosuke M Teshima, Masaya Hane, Ken Kitajima, Chihiro Sato, Naoyuki Takahata, Yoko Satta

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. 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
0.7field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Review
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

10 authors at 3 institutions in 1 country.

Toshiyuki HayakawaGraduate School of Systems Life Sciences, Kyushu University, Fukuoka, Japan.ORCID 0000-0003-3553-3555
Masahiro TeraharaGraduate School of Systems Life Sciences, Kyushu University, Fukuoka, Japan.
Naoko T FujitoSchool of Advanced Sciences, SOKENDAI (The Graduate University for Advanced Studies), Hayama, Kanagawa, Japan.
Takumi MatsunagaGraduate School of Systems Life Sciences, Kyushu University, Fukuoka, Japan.
Kosuke M TeshimaDepartment of Biology, Kyushu University, Fukuoka, Japan.ORCID 0000-0003-4854-1060
Masaya HaneBioscience and Biotechnology Center, Nagoya University, Nagoya, Aichi, Japan.
Ken KitajimaInstitute for Glyco-core Research (iGCORE), Nagoya University, Nagoya, Aichi, Japan.
Chihiro SatoInstitute for Glyco-core Research (iGCORE), Nagoya University, Nagoya, Aichi, Japan.
Naoyuki TakahataSchool of Advanced Sciences, SOKENDAI (The Graduate University for Advanced Studies), Hayama, Kanagawa, Japan.
Yoko SattaSchool of Advanced Sciences, SOKENDAI (The Graduate University for Advanced Studies), Hayama, Kanagawa, Japan.
Kyushu University · JPNagoya University · JPThe Graduate University for Advanced Studies, SOKENDAI · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ST8SIA2 is an important molecule regulating expression of the phenotype involved in schizophrenia. Lowered promoter activity of the ST8SIA2 gene is considered to be protective against schizophrenia by conferring tolerance to psychosocial stress. Here, we examined the promoter-type composition of anatomically modern humans (AMHs) and archaic humans (AHs; Neanderthals and Denisovans), and compared the promoter activity at the population level (population promoter activity; PPA) between them. In AMHs, the TCT-type, showing the second lowest promoter activity, was most prevalent in the ancestral population of non-Africans. However, the detection of only the CGT-type from AH samples and recombination tracts in AH sequences showed that the CGT- and TGT-types, exhibiting the two highest promoter activities, were common in AH populations. Furthermore, interspecies gene flow occurred into AMHs from AHs and into Denisovans from Neanderthals, influencing promoter-type compositions independently in both AMHs and AHs. The difference of promoter-type composition makes PPA unique in each population. East and Southeast Asian populations show the lowest PPA. This results from the selective increase of the CGC-type, showing the lowest promoter activity, in these populations. Every non-African population shows significantly lower PPA than African populations, resulting from the TCT-type having the highest prevalence in the ancestral population of non-Africans. In addition, PPA reduction is also found among subpopulations within Africa via a slight increase of the TCT-type. These findings indicate a trend toward lower PPA in the spread of AMHs, interpreted as a continuous adaptation to psychosocial stress arising in migration. This trend is considered as genetic tuning for the evolution of collective brains. The inferred promoter-type composition of AHs differed markedly from that of AMHs, resulting in higher PPA in AHs than in AMHs. This suggests that the trend toward lower PPA is a unique feature in AMH spread.

Indexed as

AnimalsBrainDatabases, GeneticGenetic LociHaplotypesHumansNeanderthalsPhylogenyPolymorphism, Single NucleotidePromoter Regions, GeneticSchizophreniaSialyltransferasesCMP-N-acetylneuraminate-poly-alpha-2,8-sialosyl sialyltransferaseSialyltransferases

Identifiers

PMID34914745
PMCPMC8675693
OpenAlexW4226381421

What OpenQuestion holds

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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.