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端粒酶RNA水平限制端粒长度平衡。

Telomerase RNA levels limit the telomere length equilibrium.

作者信息

Greider C W

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

Cold Spring Harb Symp Quant Biol. 2006;71:225-9. doi: 10.1101/sqb.2006.71.063.


DOI:10.1101/sqb.2006.71.063
PMID:17381301
Abstract

Small functional RNAs play essential roles in many biological processes. Regulating the level of these small RNAs can be as important as maintaining their function in cells. The telomerase RNA is maintained in cells at a steady-state level where small changes in concentration can have a profound impact on function. Cells that have half the level of the telomerase RNA cannot maintain telomeres through many cell divisions. People who are heterozygous for telomerase RNA mutations have the diseases dyskeratosis congenita and aplastic anemia, caused by short telomeres that result in loss of tissue renewal capacity. Mice heterozygous for telomerase RNA show haploinsufficiency in telomere length maintenance and also show loss of tissue renewal capacity. It is remarkable that small changes in the level of this functional RNA can have such profound effects in cells. This tight regulation highlights the importance of controlling the action of telomerase in cells.

摘要

小功能RNA在许多生物学过程中发挥着重要作用。调节这些小RNA的水平与维持它们在细胞中的功能同样重要。端粒酶RNA在细胞中以稳态水平维持,浓度的微小变化可能对功能产生深远影响。端粒酶RNA水平减半的细胞在多次细胞分裂后无法维持端粒。端粒酶RNA突变的杂合子个体患有先天性角化不良和再生障碍性贫血,这是由端粒缩短导致组织更新能力丧失引起的。端粒酶RNA杂合的小鼠在端粒长度维持方面表现出单倍剂量不足,也表现出组织更新能力丧失。值得注意的是,这种功能RNA水平的微小变化能够在细胞中产生如此深远的影响。这种严格的调控凸显了控制细胞中端粒酶作用的重要性。

相似文献

[1]
Telomerase RNA levels limit the telomere length equilibrium.

Cold Spring Harb Symp Quant Biol. 2006

[2]
Short telomeres, even in the presence of telomerase, limit tissue renewal capacity.

Cell. 2005-12-16

[3]
Stem cells, telomerase and dyskeratosis congenita.

Bioessays. 2003-2

[4]
A telomerase component is defective in the human disease dyskeratosis congenita.

Nature. 1999-12-2

[5]
Dyskeratosis congenita: telomerase, telomeres and anticipation.

Curr Opin Genet Dev. 2005-6

[6]
Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.

N Engl J Med. 2005-4-7

[7]
Dyskeratosis congenita.

Semin Hematol. 2006-7

[8]
Telomere length variation and telomerase activity expression in patients with congenital and acquired aplastic anemia.

Acta Haematol. 2004

[9]
Telomeres and aging.

Physiol Rev. 2008-4

[10]
Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complex.

Biochimie. 2008-1

引用本文的文献

[1]
Telomerase-Mediated Anti-Ageing Interventions.

Subcell Biochem. 2024

[2]
Methylation of Subtelomeric Chromatin Modifies the Expression of the lncRNA TERRA, Disturbing Telomere Homeostasis.

Int J Mol Sci. 2022-3-18

[3]
The Bur1 cyclin-dependent kinase regulates telomere length in Saccharomyces cerevisiae.

Yeast. 2022-3

[4]
Telomerase RNA processing: Implications for human health and disease.

Stem Cells. 2020-9-1

[5]
Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells.

Cell Stem Cell. 2020-6-4

[6]
, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation.

Genes Dev. 2019-9-5

[7]
Long telomeres and cancer risk: the price of cellular immortality.

J Clin Invest. 2019-8-5

[8]
Catalysis-dependent inactivation of human telomerase and its reactivation by intracellular telomerase-activating factors (iTAFs).

J Biol Chem. 2019-6-11

[9]
Insights into Telomerase/hTERT Alternative Splicing Regulation Using Bioinformatics and Network Analysis in Cancer.

Cancers (Basel). 2019-5-14

[10]
Telomerase gene expression bioassays indicate metabolic activation of genotoxic lower chlorinated polychlorinated biphenyls.

Sci Rep. 2018-11-15

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