Evidence map›Paper›PMID 39688669›Full record

ArticleGenome biology and evolution2024

Coevolution and Adaptation of Transition Nuclear Proteins and Protamines in Naturally Ascrotal Mammals Support the Black Queen Hypothesis.

Simin Chai, Jieqiong Kang, Tianzhen Wu, Yu Zheng, Xu Zhou, Shixia Xu, Wenhua Ren, Guang Yang

Abstract read
In one paragraph

Article in Genome biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Molecular divergence ofZoological research · 2026
    Article
  5. Investigating cis-regulatory elements and gene expression in multiple tomato varieties using interpretable deep learning.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
    Review
  6. Review
  7. Rapid protamine evolution suppresses meiotic drive inbioRxiv : the preprint server for biology · 2025
    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

8 authors.

Simin ChaiSouthern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou, Guangdong, China.ORCID 0000-0002-2301-5171
Jieqiong KangJiangsu Key Laboratory for Biodiversity and Biotechnology, School of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.ORCID 0009-0003-7758-5123
Tianzhen WuJiangsu Key Laboratory for Biodiversity and Biotechnology, School of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.ORCID 0009-0006-0821-6000
Yu ZhengJiangsu Key Laboratory for Biodiversity and Biotechnology, School of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.ORCID 0009-0001-5466-7762
Xu ZhouJiangsu Key Laboratory for Biodiversity and Biotechnology, School of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.ORCID 0009-0009-8522-3310
Shixia XuJiangsu Key Laboratory for Biodiversity and Biotechnology, School of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.ORCID 0000-0002-0283-0986
Wenhua RenJiangsu Key Laboratory for Biodiversity and Biotechnology, School of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.ORCID 0000-0002-8429-5963
Guang YangSouthern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou, Guangdong, China.ORCID 0000-0001-6285-6937

Funding

China Postdoctoral Science Foundation 2022M710878(Guangzhou) GML2021GD0805Guangzhou Basic and Applied Basic Research Foundation 2023A04J0770National Natural Science Foundation of China 32200345Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou)
6 · The paper itself

Abstract

Protamines (PRMs) and transition nuclear proteins (TNPs) are two key classes of sperm nuclear basic proteins that regulate chromatin reorganization and condensation in the spermatozoon head, playing crucial roles in mammalian spermatogenesis. In scrotal mammals, such as humans, cryptorchidism, the failure of the testes to descend into the scrotal sac is generally associated with higher rates of defective spermatozoon quality and function. However, ascrotal mammals, such as cetaceans, with naturally undescended testes, produce normal spermatozoa similar to their scrotal counterparts. This study investigates the evolutionary pattern and functional changes in PRMs and TNPs to explore the potential molecular mechanisms underlying spermatogenesis in naturally ascrotal mammals. Although we found a conserved genomic arrangement for PRM and TNP genes across mammals, the coevolutionary loss of intact PRM2 and TNP2 was observed in several species, correlating significantly with diverse testicular positions. Notably, in cetaceans, which lack intact PRM2 and TNP2, we detected enhanced thermostability and DNA binding in PRM1, along with superior DNA repair capability in TNP1. These findings suggest that gene loss of PRM2 and TNP2, combined with functional enhancements in PRM1 and TNP1 proteins, evolved in response to physiological challenges posed by natural cryptorchidism in most ascrotal lineages. This evolutionary strategy enhances chromatin condensation efficiency and promotes DNA repair during spermatogenesis in natural cryptorchid mammals, supporting the Black Queen Hypothesis.

Indexed as

Evolution, MolecularProtaminesSpermatogenesisAnimalsCetaceaHumansMaleMammalsNuclear ProteinsPhylogenySpermatozoaNuclear ProteinsProtaminesascrotal mammalprotaminethe black queen hypothesistransition nuclear protein

Identifiers

PMID39688669
PMCPMC11652718

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