Evidence map›Paper›PMID 41166362›Full record

ArticlePLoS genetics2025

Dosage-dependent regulation of embryonic diapause by sorbitol dehydrogenase in the silkworm, Bombyx mori.

Dongbin Chen, Dehong Yang, Xin Fu, Haixu Bian, Yongping Huang, Yanqun Liu, Zulian Liu

Abstract read
In one paragraph

Article in PLoS genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Dongbin ChenSchool of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, China.ORCID https://orcid.org/0009-0003-8396-1025
Dehong YangSchool of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, China.
Xin FuDepartment of Sericulture, College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang, China.
Haixu BianDepartment of Sericulture, College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang, China.
Yongping HuangSchool of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, China.ORCID https://orcid.org/0000-0002-3266-1327
Yanqun LiuDepartment of Sericulture, College of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang, China.ORCID https://orcid.org/0000-0001-9025-1986
Zulian LiuSchool of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, China.ORCID https://orcid.org/0000-0001-7942-8322

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insects have evolved diapause to cope with harsh environmental conditions, during which their metabolism undergoes significant remodeling. The silkworm, Bombyx mori, enters diapause in the early embryonic stage, a process critically regulated by the sorbitol metabolism pathway and its key enzyme, sorbitol dehydrogenase (SDH). Nevertheless, the precise involvement of SDH in the diapause regulation of the silkworm remains to be fully understood. In this study, we identified that BmSdh2 is highly expressed in diapause-destined silkworm embryos through RNA-seq analysis. Genetic manipulation of BmSdh2 expression significantly influenced diapause progression: complete homozygous knockout of BmSdh2 led to diapause termination, whereas partial loss-of-function mutations maintained the wild-type diapause phenotype. Furthermore, integrative LC-MS/MS, metabolomic, and lipidomic analyses demonstrated that BmSdh2 dosage critically modulates diapause maintenance. These findings highlight BmSdh2 as a novel and potentially central molecular regulator in the silkworm diapause pathway.

Indexed as

BombyxDiapauseDiapause, InsectInsect ProteinsL-Iditol 2-DehydrogenaseAnimalsEmbryo, NonmammalianGene DosageGene Expression Regulation, DevelopmentalInsect ProteinsL-Iditol 2-Dehydrogenase

Identifiers

PMID41166362
PMCPMC12594423

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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.