Evidence map›Paper›PMID 35642306›Full record

ArticleMolecular biology and evolution2022

How Placenta Promotes the Successful Reproduction in High-Altitude Populations: A Transcriptome Comparison between Adaptation and Acclimatization.

Deng Wu, Yunao Liu, Wei Chen, Jianming Shao, Pubu Zhuoma, Dexiong Zhao, Yang Yu, Tianzi Liu, Ruoxuan Yu, Yongna Gan and 13 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Molecular biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Dysregulated Fatty Acid Metabolism in Preeclampsia Among Highland Andeans: Insights Into Adaptive and Maladaptive Placental Metabolic Phenotypes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. The uteroplacental circulation at high altitude: adaptation and maladaptation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  6. Article
  7. Article
  8. Placental Adaptation to Hypoxia: The Case of High-Altitude Pregnancies.International journal of environmental research and public health · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Adaptive structural and functional evolution of the placenta protects fetal growth in high-elevation deer mice.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Allometric scaling relationships in mouse placenta.Journal of the Royal Society, Interface · 2022
    Article
  16. 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

23 authors at 4 institutions in 1 country.

Deng WuThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.ORCID 0000-0003-3144-2007
Yunao LiuThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Wei ChenThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Jianming ShaoThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Pubu ZhuomaDepartment of Obstetrics and Gynecology, The Second People's Hospital of Tibet Autonomous Region, Lhasa, Tibet, China.
Dexiong ZhaoDepartment of Obstetrics and Gynecology, Qinghai Red Cross Hospital, Xining, Qinghai, China.
Yang YuCenter for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, China.ORCID 0000-0002-4310-1966
Tianzi LiuThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Ruoxuan YuState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Yongna GanDepartment of Obstetrics and Gynecology, Qinghai Red Cross Hospital, Xining, Qinghai, China.
Baima YuzhengDepartment of Obstetrics and Gynecology, The Second People's Hospital of Tibet Autonomous Region, Lhasa, Tibet, China.
Yongshu HuangDepartment of Obstetrics and Gynecology, The Second People's Hospital of Tibet Autonomous Region, Lhasa, Tibet, China.
Haikun ZhangThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Xiaoman BiThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Chengcheng TaoThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Shujuan LaiThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Qiaoxia LuoThe Third People's Hospital of Tibet Autonomous Region, Lhasa, Tibet, China.
Dake ZhangThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Hongmei WangState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Pingcuo ZhaxiThe Third People's Hospital of Tibet Autonomous Region, Lhasa, Tibet, China.
Jianqing ZhangDepartment of Obstetrics and Gynecology, The Second People's Hospital of Tibet Autonomous Region, Lhasa, Tibet, China.
Jie QiaoCenter for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, China.ORCID 0000-0003-2126-1376
Changqing ZengThe Key Laboratory of Precision and Genomic Medicine, Chinese Academy of Sciences; Beijing Institute of Genomics (China National Center for Bioinformation), University of Chinese Academy of Sciences, Beijing, China.
Chinese Academy of Sciences · CNTibet Autonomous Region People's Hospital · CNPeking University · CNQinghai Red Cross Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the best adapted high altitude population, Tibetans feature a relatively high offspring survival rate. Genome-wide studies have identified hundreds of candidate SNPs related to high altitude adaptation of Tibetans, although most of them have unknown functional relevance. To explore the mechanisms behind successful reproduction at high altitudes, we compared the placental transcriptomes of Tibetans, sea level Hans (SLHan), and Han immigrants (ImHan). Among the three populations, placentas from ImHan showed a hyperactive gene expression pattern. Their increased activation demonstrates a hypoxic stress response similar to sea level individuals experiencing hypoxic conditions. Unlike ImHan, Tibetan placentas were characterized by the significant up-regulation of placenta-specific genes, and the activation of autophagy and the tricarboxylic acid (TCA) cycle. Certain conserved hypoxia response functions, including the antioxidant system and angiogenesis, were activated in both ImHan and Tibetans, but mediated by different genes. The coherence of specific transcriptome features linked to possible genetic contribution was observed in Tibetans. Furthermore, we identified a novel Tibetan-specific EPAS1 isoform with a partial deletion at exon six, which may be involved in the adaption to hypoxia through the EPAS1-centred gene network in the placenta. Overall, our results show that the placenta grants successful pregnancies in Tibetans by strengthening the natural functions of the placenta itself. On the other hand, the placenta of ImHan was in an inhabiting time-dependent acclimatization process representing a common hypoxic stress response pattern.

Indexed as

AltitudeTranscriptomeAcclimatizationFemaleHemoglobinsHumansHypoxiaPlacentaPregnancyReproductionTibetHemoglobinsacclimatizationadaptationhypoxiaplacentaTibetanstranscriptome

Identifiers

PMID35642306
PMCPMC9206416
OpenAlexW4281745177

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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.