Evidence map›Paper›PMID 35794099›Full record

ArticleNature communications2022

Comparison of chromatin accessibility landscapes during early development of prefrontal cortex between rhesus macaque and human.

Xuelong Yao, Zongyang Lu, Zhanying Feng, Lei Gao, Xin Zhou, Min Li, Suijuan Zhong, Qian Wu, Zhenbo Liu, Haofeng Zhang and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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    Article
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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

19 authors at 7 institutions in 1 country.

Xuelong Yao *CAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, 100101, Beijing, China.
Zongyang Lu *University of Chinese Academy of Sciences, 100049, Beijing, China.
Zhanying Feng *University of Chinese Academy of Sciences, 100049, Beijing, China.ORCID 0000-0002-5727-3929
Lei Gao *CAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, 100101, Beijing, China.
Xin ZhouState Key Laboratory of Brain and Cognitive Science, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Brain-Intelligence Technology (Shanghai), Institute of Biophysics, Chinese Academy of Sciences, 100101, Beijing, China.
Min LiUniversity of Chinese Academy of Sciences, 100049, Beijing, China.
Suijuan ZhongState Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, 100875, Beijing, China.
Qian WuState Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, 100875, Beijing, China.ORCID 0000-0002-7469-1583
Zhenbo LiuCAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, 100101, Beijing, China.
Haofeng ZhangObstetrics and Gynecology Medical Center of Severe Cardiovascular of Beijing Anzhen Hospital, Capital Medical University, 100029, Beijing, China.
Zeyuan LiuUniversity of Chinese Academy of Sciences, 100049, Beijing, China.
Lizhi YiCAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, 100101, Beijing, China.
Tao ZhouSchool of Life Science and Technology, Shanghai Tech University, 100 Haike Rd., Pudong New Area, Shanghai, 201210, China.ORCID 0000-0002-3933-0643
Xudong ZhaoKunming Primate Research Center, Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences, Kunming Institute of Zoology, Chinese Academy of Sciences, 650223, Kunming, China.ORCID 0000-0001-9126-7365
Jun ZhangObstetrics and Gynecology Medical Center of Severe Cardiovascular of Beijing Anzhen Hospital, Capital Medical University, 100029, Beijing, China.
Yong WangUniversity of Chinese Academy of Sciences, 100049, Beijing, China.ORCID 0000-0003-0695-5273
Xingxu HuangSchool of Life Science and Technology, Shanghai Tech University, 100 Haike Rd., Pudong New Area, Shanghai, 201210, China. huangxx@shanghaitech.edu.cn.ORCID 0000-0001-8934-1247
Xiaoqun WangUniversity of Chinese Academy of Sciences, 100049, Beijing, China. xiaoqunwang@ibp.ac.cn.ORCID 0000-0003-3440-2617
Jiang LiuCAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, 100101, Beijing, China. liuj@big.ac.cn.ORCID 0000-0002-5687-5047
Chinese Academy of Sciences · CNShanghaiTech University · CNBeijing Normal University · CNCapital Medical University · CNCenter for Excellence in Brain Science and Intelligence Technology · CNKunming Institute of Zoology · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epigenetic information regulates gene expression and development. However, our understanding of the evolution of epigenetic regulation on brain development in primates is limited. Here, we compared chromatin accessibility landscapes and transcriptomes during fetal prefrontal cortex (PFC) development between rhesus macaques and humans. A total of 304,761 divergent DNase I-hypersensitive sites (DHSs) are identified between rhesus macaques and humans, although many of these sites share conserved DNA sequences. Interestingly, most of the cis-elements linked to orthologous genes with dynamic expression are divergent DHSs. Orthologous genes expressed at earlier stages tend to have conserved cis-elements, whereas orthologous genes specifically expressed at later stages seldom have conserved cis-elements. These genes are enriched in synapse organization, learning and memory. Notably, DHSs in the PFC at early stages are linked to human educational attainment and cognitive performance. Collectively, the comparison of the chromatin epigenetic landscape between rhesus macaques and humans suggests a potential role for regulatory elements in the evolution of differences in cognitive ability between non-human primates and humans.

Indexed as

ChromatinEpigenesis, GeneticAnimalsDeoxyribonuclease IHumansMacaca mulattaPrefrontal CortexRegulatory Sequences, Nucleic AcidChromatinDeoxyribonuclease I

Identifiers

PMID35794099
PMCPMC9259620
OpenAlexW4283832436

What Socratic 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 Socratic graph.