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端粒结合蛋白Taz1在端粒处独立于RNA干扰建立Swi6异染色质。

Telomere binding protein Taz1 establishes Swi6 heterochromatin independently of RNAi at telomeres.

作者信息

Kanoh Junko, Sadaie Mahito, Urano Takeshi, Ishikawa Fuyuki

机构信息

Department of Gene Mechanisms, Graduate School of Biostudies, Kyoto University, Kitashirakawaoiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan.

出版信息

Curr Biol. 2005 Oct 25;15(20):1808-19. doi: 10.1016/j.cub.2005.09.041.

Abstract

BACKGROUND

The telomere is a specialized heterochromatin conserved among eukaryotes. However, it remains unknown how heterochromatin protein 1 (HP1) is recruited to telomeres and how telomere heterochromatin is formed. In fission yeast, the RNAi (RNA interference)-RITS (RNA-induced initiation of transcriptional silencing) pathway initiates heterochromatin formation at the centromeres and the silent mat locus by using common DNA sequences, the dg and dh repeats, as the templates for small interfering RNA (siRNA).

RESULTS

We found that telomeric repeats are sufficient for the establishment of Swi6 (a fission-yeast HP1 homolog) heterochromatin, and the establishment requires Taz1, a telomere binding protein of the TRF family. Additionally, Swi6 heterochromatin is established by a part of the subtelomere that contains sequences highly homologous to that of the dh repeat, and it is strikingly destabilized by the deletion of both Taz1 and RNAi-RITS. Transcripts from the telomeric dh-homologous region were specifically associated with RITS, and deletion of the telomeric dh-homologous region showed the phenotype similar to that of the rnai mutant in terms of the telomeric silencing, indicating that the RNAi-RITS pathway acts at the telomeric dh-homologous region to establish Swi6 heterochromatin. Furthermore, we found that Taz1 establishes Swi6 heterochromatin independently of the telomeric repeats and the RNAi-RITS pathway at the subtelomeres.

CONCLUSION

The telomere heterochromatin is regulated by at least two factors: One is Taz1, which is telomere specific, and the other is RNAi-RITS, which is commonly used at the constitutive heterochromatin regions.

摘要

背景

端粒是真核生物中保守的一种特殊异染色质。然而,异染色质蛋白1(HP1)如何被招募到端粒以及端粒异染色质如何形成仍不清楚。在裂殖酵母中,RNA干扰(RNAi)-RNA诱导的转录沉默(RITS)途径通过使用常见的DNA序列dg和dh重复序列作为小干扰RNA(siRNA)的模板,在着丝粒和沉默的mat位点启动异染色质形成。

结果

我们发现端粒重复序列足以建立Swi6(裂殖酵母HP1同源物)异染色质,并且该建立过程需要Taz1,一种TRF家族的端粒结合蛋白。此外,Swi6异染色质是由包含与dh重复序列高度同源序列的一部分亚端粒建立的,并且通过删除Taz1和RNAi-RITS两者会使其显著不稳定。来自端粒dh同源区域的转录本与RITS特异性相关,并且删除端粒dh同源区域在端粒沉默方面表现出与RNAi突变体相似的表型,表明RNAi-RITS途径在端粒dh同源区域起作用以建立Swi6异染色质。此外,我们发现在亚端粒处Taz1独立于端粒重复序列和RNAi-RITS途径建立Swi6异染色质。

结论

端粒异染色质受至少两个因素调节:一个是Taz1,它是端粒特异性的,另一个是RNAi-RITS,它在组成型异染色质区域普遍使用。

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