Evidence map›Paper›PMID 38609871›Full record

ArticleBMC genomics2024

Comparative transcriptomic analysis delineates adaptation strategies of Rana kukunoris toward cold stress on the Qinghai-Tibet Plateau.

Tao Zhang, Lun Jia, Zhiyi Niu, Xinying Li, Shengkang Men, Lu Jiang, Miaojun Ma, Huihui Wang, Xiaolong Tang, Qiang Chen

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Tao ZhangDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China.
Lun JiaDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China.
Zhiyi NiuDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China.
Xinying LiDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China.
Shengkang MenDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China.
Lu JiangDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China.
Miaojun MaState Key Laboratory of Herbage Improvement and Grassland Agro-ecosystems, College of Ecology, Lanzhou University, Lanzhou, China.
Huihui WangSchool of Stomatology, Lanzhou University, Lanzhou, China.
Xiaolong TangDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China. tangxl@lzu.edu.cn.
Qiang ChenDepartment of Animal and Biomedical Sciences, School of Life Sciences, Lanzhou University, Lanzhou, China. chenq@lzu.edu.cn.
Lanzhou University · CN

Funding

the Fundamental Research Funds for the Central Universities lzujbky-2022-55the National Natural Science Foundation of China 31971416the National Natural Science Foundation of China 32301311
6 · The paper itself

Abstract

backgroundCold hardiness is fundamental for amphibians to survive during the extremely cold winter on the Qinghai-Tibet plateau. Exploring the gene regulation mechanism of freezing-tolerant Rana kukunoris could help us to understand how the frogs survive in winter.

resultsTranscriptome of liver and muscle of R. kukunoris collected in hibernation and spring were assisted by single molecule real-time (SMRT) sequencing technology. A total of 10,062 unigenes of R. kukunoris were obtained, and 9,924 coding sequences (CDS) were successfully annotated. Our examination of the mRNA response to whole body freezing and recover in the frogs revealed key genes concerning underlying antifreeze proteins and cryoprotectants (glucose and urea). Functional pathway analyses revealed differential regulated pathways of ribosome, energy supply, and protein metabolism which displayed a freeze-induced response and damage recover. Genes related to energy supply in the muscle of winter frogs were up-regulated compared with the muscle of spring frogs. The liver of hibernating frogs maintained modest levels of protein synthesis in the winter. In contrast, the liver underwent intensive high levels of protein synthesis and lipid catabolism to produce substantial quantity of fresh proteins and energy in spring. Differences between hibernation and spring were smaller than that between tissues, yet the physiological traits of hibernation were nevertheless passed down to active state in spring.

conclusionsBased on our comparative transcriptomic analyses, we revealed the likely adaptive mechanisms of R. kukunoris. Ultimately, our study expands genetic resources for the freezing-tolerant frogs.

Indexed as

Cold-Shock ResponseTranscriptomeAnimalsAnuraGene Expression ProfilingRanidaeTibetEmergence periodFreeze exposureHibernationLiverMusclePacbio sequelTissue specificity

Identifiers

PMID38609871
PMCPMC11015565
OpenAlexW4394750048

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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.