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相关概念视频

Telomeres and Telomerase02:41

Telomeres and Telomerase

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In eukaryotic DNA replication, a single-stranded DNA fragment remains at the end of a chromosome after the removal of the final primer. This section of DNA cannot be replicated in the same manner as the rest of the strand because there is no 3’ end to which the newly synthesized DNA can attach. This non-replicated fragment results in gradual loss of the chromosomal DNA during each cell duplication. Additionally, it can induce a DNA damage response by enzymes that recognize single-stranded...
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Replicative Cell Senescence02:15

Replicative Cell Senescence

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Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds...
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Replication in Eukaryotes01:29

Replication in Eukaryotes

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In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
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Mitochondria01:37

Mitochondria

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Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
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Aging01:26

Aging

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Aging is a complex biological phenomenon influenced by various processes that affect cellular and systemic functions. Several prominent theories attempt to explain its mechanisms, highlighting cellular limitations, oxidative damage, and hormonal changes as central factors in aging.
Cellular Clock Theory
The cellular clock theory posits that the human lifespan is closely tied to the finite capacity of cells to divide, a phenomenon governed by telomeres, which are protective caps at the ends of...
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Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

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Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
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相关实验视频

Updated: Jun 4, 2025

Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer
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Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer

Published on: April 13, 2015

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端粒酶介导的抗衰老干预措施

Phoebe L Dunn1, Dhenugen Logeswaran2, Julian J-L Chen3

  • 1School of Life Sciences, Arizona State University, Tempe, Arizona, USA.

Sub-cellular biochemistry
|December 18, 2024
PubMed
概括

防止端粒缩短可能会延迟衰老. 研究了增加端粒酶水平或活性的策略,提供潜在的抗衰老益处,但需要仔细分析风险和益处.

科学领域:

  • 细胞生物学 细胞生物学
  • 遗传学 遗传学 是一个
  • 老年学是一门学科.

背景情况:

  • 细胞衰老与染色体完整性下降和端粒缩短有关.
  • 端粒,保护性DNA帽子,由于最终复制问题,随着复制而缩短.
  • 端粒酶对抗这种缩短,保持特定细胞的端粒长度.

研究的目的:

  • 审查针对端粒缩短的抗衰老干预措施.
  • 分析增加端粒酶水平或活性的策略.
  • 讨论这些干预措施的风险,好处和未来.

主要方法:

  • 对抗衰老策略的文献综述.
  • 对端粒生物学和端粒酶功能的分析.
  • 讨论细胞衰老作为衰老的标志.

主要成果:

  • 在体细胞中逐渐缩短端粒导致细胞衰老.
  • 衰老细胞的积累有助于生物体的衰老.
  • 防止端粒缩短是一种潜在的抗衰老方法.

结论:

  • 增加端粒酶活性是缓解衰老的一个有希望的策略.
关键词:
细胞衰老 细胞衰老复制DNA复制DNA复制DNA复制结束复制问题 结束复制问题草的限制值是什么核糖蛋白是一种核糖蛋白.端粒酶激活的激活方式端粒缩短的原因是

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Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence
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Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence

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Telomerase Activity in the Various Regions of Mouse Brain: Non-Radioactive Telomerase Repeat Amplification Protocol TRAP Assay
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Telomerase Activity in the Various Regions of Mouse Brain: Non-Radioactive Telomerase Repeat Amplification Protocol TRAP Assay

Published on: September 2, 2014

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相关实验视频

Last Updated: Jun 4, 2025

Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer
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Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer

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Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence
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Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence

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Telomerase Activity in the Various Regions of Mouse Brain: Non-Radioactive Telomerase Repeat Amplification Protocol TRAP Assay
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Telomerase Activity in the Various Regions of Mouse Brain: Non-Radioactive Telomerase Repeat Amplification Protocol TRAP Assay

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  • 仔细考虑风险和益处对于治疗开发至关重要.
  • 需要进一步的研究来优化针对端粒的抗衰老干预措施.