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Updated: Apr 27, 2026

Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence
Published on: May 22, 2013
Telomere and telomerase biology
Miriam Aparecida Giardini1, Marcela Segatto1, Marcelo Santos da Silva1
1Depto. de Genética, Instituto de Biociências, Univ. Estadual Paulista Júlio de Mesquita Filho UNESP-Botucatu, São Paulo, Brazil.
Telomeres protect chromosome ends through repetitive DNA and proteins. Telomere dysfunction, due to lack of telomerase or protein defects, causes aging, genetic disorders, and genomic instability.
Area of Science:
- Molecular Biology
- Genetics
- Cell Biology
Background:
- Telomeres are protective caps at the ends of linear chromosomes.
- They prevent degradation and distinguish chromosome ends from DNA breaks.
- Telomeres consist of repetitive DNA and associated proteins forming dynamic complexes.
Purpose of the Study:
- To review the mechanisms of telomere maintenance and length regulation.
- To discuss the consequences of telomere dysfunction in various cellular contexts.
- To highlight the role of telomerase, alternative lengthening of telomeres, and telomeric repeat-containing RNA.
Main Methods:
- Review of existing literature on telomere biology.
- Analysis of the roles of telomerase and alternative lengthening of telomeres.
- Examination of the impact of telomere protein depletion and genetic mutations.
Main Results:
- Telomere shortening occurs in aging mammalian somatic cells, leading to senescence.
- Defects in telomere components can cause inherited disorders and chromosomal abnormalities.
- Long noncoding RNAs from subtelomeric regions also influence telomere maintenance.
Conclusions:
- Understanding telomere homeostasis is crucial for addressing genomic instability and genetic diseases.
- Further research is needed to elucidate regulatory mechanisms and the impact of telomere dysfunction.
- Telomere integrity is essential for preventing severe genetic disorders and maintaining genomic stability.
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