Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

The Effect of Aging on Tissues01:19

The Effect of Aging on Tissues

3.3K
Several body functions deteriorate with age. The external signs of aging are easily identifiable. For example, the skin becomes dry, less elastic, and thins out, forming wrinkles. The skin of the face begins to appear looser due to a decrease in the levels of elastic and collagen fibers in the connective tissue. Additionally, melanin production in the hair follicle decreases with age, resulting in gray hair. Moreover, the senses of sight and hearing decline, so glasses and hearing aids may...
3.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

PTEN Loss Promotes PI3Kβ Phosphorylation and EPHA2/SRC/p-PI3KβY962 Complex Assembly to Drive Tumorigenesis.

Cancer discovery·2025
Same author

Effective in vivo RNA base editing via engineered cytidine deaminase APOBECs fused with PUF proteins.

Nature communications·2025
Same author

Author Correction: Interplay of genetic predisposition, plasma metabolome and Mediterranean diet in dementia risk and cognitive function.

Nature medicine·2025
Same author

When biomedical discovery faces data barriers: building a governance-empowered framework for resilient collaboration.

Molecular systems biology·2025
Same author

Interplay of genetic predisposition, plasma metabolome and Mediterranean diet in dementia risk and cognitive function.

Nature medicine·2025
Same author

Boosting RNA nanotherapeutics with V-ATPase activating non-inflammatory lipid nanoparticles to treat chronic lung injury.

Nature communications·2025
Same journal

Canonical and phosphoribosyl ubiquitination coordinate to stabilize a proteinaceous structure surrounding the <i>Legionella</i>-containing vacuole.

eLife·2026
Same journal

Celldetective, an AI-enhanced image analysis tool for unraveling dynamic cell interactions.

eLife·2026
Same journal

Dynamic assembly of malate dehydrogenase-citrate synthase multienzyme complex in the mitochondria.

eLife·2026
Same journal

Autosomal allelic inactivation at loci with variable replication timing and dosage sensitivity.

eLife·2026
Same journal

Cribriform plate microenvironment assembles a suppressive myeloid network during EAE-induced neuroinflammation.

eLife·2026
Same journal

Proteomic composition and mutual assembly of the C2a projection in vertebrate motile cilia.

eLife·2026
See all related articles

Related Experiment Video

Updated: Jan 16, 2026

Author Spotlight: Exploring Sex-Specific Glial Signatures and Therapeutic Leads for Alzheimer&#39;s Disease
04:22

Author Spotlight: Exploring Sex-Specific Glial Signatures and Therapeutic Leads for Alzheimer's Disease

Published on: May 20, 2024

1.3K

Pan-tissue transcriptome analysis reveals sex-dimorphic human aging.

Siqi Wang1,2, Danyue Dong1, Xin Li1

  • 1Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.

Elife
|October 3, 2025
PubMed
Summary
This summary is machine-generated.

This study reveals significant sex differences in aging across 35 human tissues, impacting gene expression and alternative splicing (AS). Male aging shows earlier, larger transcriptome changes linked to sex hormones and Alzheimer's disease risk.

Keywords:
AS regulatory networkagingalternative splicingchromosomescomputational biologygene expressionhumansex dimorphismsystems biologytime series

More Related Videos

Cell-Specific Paired Interrogation of the Mouse Ovarian Epigenome and Transcriptome
12:25

Cell-Specific Paired Interrogation of the Mouse Ovarian Epigenome and Transcriptome

Published on: February 24, 2023

1.2K
Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts
07:03

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts

Published on: January 2, 2018

6.6K

Related Experiment Videos

Last Updated: Jan 16, 2026

Author Spotlight: Exploring Sex-Specific Glial Signatures and Therapeutic Leads for Alzheimer&#39;s Disease
04:22

Author Spotlight: Exploring Sex-Specific Glial Signatures and Therapeutic Leads for Alzheimer's Disease

Published on: May 20, 2024

1.3K
Cell-Specific Paired Interrogation of the Mouse Ovarian Epigenome and Transcriptome
12:25

Cell-Specific Paired Interrogation of the Mouse Ovarian Epigenome and Transcriptome

Published on: February 24, 2023

1.2K
Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts
07:03

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts

Published on: January 2, 2018

6.6K

Area of Science:

  • Genomics
  • Aging Research
  • Sex Differences in Medicine

Background:

  • Complex diseases show sex dimorphism in outcomes, often linked to aging.
  • Mechanisms of sex-dimorphic aging across multiple tissues are poorly understood.

Purpose of the Study:

  • To quantitatively assess sex and age contributions to transcriptomic variation across 35 human tissues.
  • To uncover molecular mechanisms underlying sex-dimorphic aging patterns.

Main Methods:

  • Systematic analysis of ~17,000 transcriptomes from 35 human tissues.
  • Evaluation of gene expression and alternative splicing (AS) changes related to sex and age.
  • Breakpoint analysis to associate aging rates with sex hormone levels.

Main Results:

  • Extensive sex dimorphisms observed in aging transcriptomes with distinct patterns in gene expression and AS.
  • Male-biased age-associated AS events correlate with Alzheimer's disease risk.
  • Female-biased AS events potentially regulated by estrogen receptor pathways.
  • Sex-dimorphic aging rates linked to sex hormone decline; males exhibit earlier and more pronounced transcriptome changes.

Conclusions:

  • Sex plays a critical role in aging at molecular and multi-tissue levels.
  • Identified sex-dimorphic regulatory patterns provide insights into age-related diseases.
  • Findings highlight the importance of considering sex in aging research and clinical applications.