Evidence map›Paper›PMID 40244140›Full record

ReviewInternational journal of molecular sciences2025

The Cause-Effect Model of Master Sex Determination Gene Acquisition and the Evolution of Sex Chromosomes.

Zhanjiang Liu, Dongya Gao

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Zhanjiang LiuDepartment of Biology, College of Arts and Sciences, Tennessee Technological University, Cookeville, TN 38505, USA.ORCID 0000-0003-3495-135X
Dongya GaoDepartment of Biology, College of Arts and Sciences, Tennessee Technological University, Cookeville, TN 38505, USA.

Funding

United States Department of Agriculture 2023-67015-41839
6 · The paper itself

Abstract

The canonical model of vertebrate sex chromosome evolution predicts a one-way trend toward degradation. However, most sex chromosomes in lower vertebrates are homomorphic. Recent progress in studies of sex determination has resulted in the discovery of more than 30 master sex determination (MSD) genes, most of which are from teleost fish. An analysis of MSD gene acquisition, recombination suppression, and sex chromosome-specific sequences revealed correlations in the modes of MSD gene acquisition and the evolution of sex chromosomes. Sex chromosomes remain homomorphic with MSD genes acquired by simple mutations, gene duplications, allelic variations, or neofunctionalization; in contrast, they become heteromorphic with MSD genes acquired by chromosomal inversion, fusion, and fission. There is no recombination suppression with sex chromosomes carrying MSD genes gained through simple mutations. In contrast, there is extensive recombination suppression with sex chromosomes carrying MSD genes gained through chromosome inversion. There is limited recombination suppression with sex chromosomes carrying MSD genes gained through transposition or translocation. We propose a cause-effect model that predicts sex chromosome evolution as a consequence of the acquisition modes of MSD genes, which explains the evolution of sex chromosomes in various vertebrates. A key factor determining the trend of sex chromosome evolution is whether non-homologous regions are created during the acquisition of MSD genes. Chromosome inversion creates inversely homologous but directly non-homologous sequences, which lead to recombination suppression but retain recombination potential. Over time, recurrent recombination in the inverted regions leads to the formation of strata and may cause the degradation of sex chromosomes. Depending on the nature of deletions in the inverted regions, sex chromosomes may evolve with dosage compensation, or the selective retention of haplo-insufficient genes may be used as an alternative strategy.

Indexed as

Evolution, MolecularModels, GeneticSex ChromosomesSex Determination ProcessesAnimalsFemaleHumansMaleRecombination, Geneticchromosome inversionmaster sex determination generecombination suppressionsex chromosome evolutionsex determinationsex differentiation

Identifiers

PMID40244140
PMCPMC11989894

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