Jump to content

Hallmarks of Aging: Difference between revisions

Line 187: Line 187:
|Telomere shortening is associated with a variety of human diseases, including pulmonary fibrosis, dyskeratosis congenita, and aplastic anemia, often linked to deficiencies in telomerase or shelterin components{{pmid|22965356}}.
|Telomere shortening is associated with a variety of human diseases, including pulmonary fibrosis, dyskeratosis congenita, and aplastic anemia, often linked to deficiencies in telomerase or shelterin components{{pmid|22965356}}.
|-
|-
| rowspan="3" style="text-align:center; background-color:hsla(180, 100%, 85%);" |[[File:Epigenome-transparent-upscale.png|frameless|85x85px]]
| rowspan="4" style="text-align:center; background-color:hsla(180, 100%, 85%);" |[[File:Epigenome-transparent-upscale.png|frameless|85x85px]]
| rowspan="3" style="background-color:hsla(180, 100%, 85%);" |'''[[Epigenetic Alterations|Epigenetic alterations]]'''
| rowspan="4" style="background-color:hsla(180, 100%, 85%);" |'''[[Epigenetic Alterations|Epigenetic alterations]]'''
| style="background-color:hsla(180, 100%, 85%);" |'''Histone modifications''' are a type of epigenetic alteration that play a crucial role in regulating gene expression. Histones are proteins around which DNA is wrapped in eukaryotic cells, forming a structure known as a nucleosome. These modifications occur primarily at the tails of histone proteins and influence how tightly or loosely DNA is wound around the histones, affecting the accessibility of the DNA to various cellular machinery for processes like transcription, replication, and repair.
| style="background-color:hsla(180, 100%, 85%);" |'''Histone modifications''' are a type of epigenetic alteration that play a crucial role in regulating gene expression. Histones are proteins around which DNA is wrapped in eukaryotic cells, forming a structure known as a nucleosome. These modifications occur primarily at the tails of histone proteins and influence how tightly or loosely DNA is wound around the histones, affecting the accessibility of the DNA to various cellular machinery for processes like transcription, replication, and repair.
|Chemical changes to histone proteins after they are formed can activate or silence gene expression and regulate the aging process.{{pmid|17320507}}
|Chemical changes to histone proteins after they are formed can activate or silence gene expression and regulate the aging process.{{pmid|17320507}}
Line 212: Line 212:
|
|
|-
|-
|'''Chromatin remodeling''':
|'''Transcriptional alterations''' refer to changes in the process by which genes are expressed into RNA, which can then be translated into proteins. These alterations can influence which genes are turned on or off, the timing of their activation, the amount of RNA produced, and the stability or processing of that RNA.
|Chromatin remodeling, involving chromosomal proteins and factors like HP1α and Polycomb group proteins, changes with age. These alterations contribute to global heterochromatin loss and affect chromosomal stability{{pmid|19734887}} {{pmid|22647267}}.
|Aging leads to more transcriptional noise, meaning more random variations in gene activity{{pmid|16791200}}, and also causes irregular production and processing of many mRNAs, the molecules that carry genetic information from DNA for protein creation{{pmid|21668623}}{{pmid|20538013}}. Also miRNAs that is associated with the aging process is affected{{pmid|22660319}}{{pmid|22064465}}.
|Disruptions in chromatin remodeling factors can accelerate aging, as shown in models with loss-of-function mutations in key proteins like HP1α{{pmid|22291607}}.
|Expression of several miRNAs increases longevity in [[Drosophila Melanogaster|Drosophila melanogaster]] and [[Nematode Worms (Caenorhabditis Elegans)|C. elegans]]{{pmid|22343898}}{{pmid|23239738}}{{pmid|22294612}}.
|Manipulating chromatin remodeling components may slow aging, as indicated by the extended lifespan in flies with overexpressed heterochromatin proteins{{pmid|22291607}}.
|Loss of several miRNAs is associated with increase aging in [[Drosophila Melanogaster|Drosophila melanogaster]] and [[Nematode Worms (Caenorhabditis Elegans)|C. elegans]]{{pmid|22343898}}{{pmid|23239738}}{{pmid|22294612}}.
|Alterations in chromatin remodeling are implicated in various age-related diseases and conditions, impacting genomic stability and cellular functionality{{pmid|19734887}}.
|
|-
|-
| style="text-align:center; background-color:hsla(210, 100%, 85%);" |[[File:Stress signaling.png|frameless|95x95px]]
| style="text-align:center; background-color:hsla(210, 100%, 85%);" |[[File:Stress signaling.png|frameless|95x95px]]
Cookies help us deliver our services. By using our services, you agree to our use of cookies.