کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1946506 1537279 2013 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Transcription reinitiation by RNA polymerase III
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Transcription reinitiation by RNA polymerase III
چکیده انگلیسی

The retention of transcription proteins at an actively transcribed gene contributes to maintenance of the active transcriptional state and increases the rate of subsequent transcription cycles relative to the initial cycle. This process, called transcription reinitiation, generates the abundant RNAs in living cells. The persistence of stable preinitiation intermediates on activated genes representing at least a subset of basal transcription components has long been recognized as a shared feature of RNA polymerase (Pol) I, II and III-dependent transcription in eukaryotes. Studies of the Pol III transcription machinery and its target genes in eukaryotic genomes over the last fifteen years, has uncovered multiple details on transcription reinitiation. In addition to the basal transcription factors that recruit the polymerase, Pol III itself can be retained on the same gene through multiple transcription cycles by a facilitated recycling pathway. The molecular bases for facilitated recycling are progressively being revealed with advances in structural and functional studies. At the same time, progress in our understanding of Pol III transcriptional regulation in response to different environmental cues points to the specific mechanism of Pol III reinitiation as a key target of signaling pathway regulation of cell growth. This article is part of a Special Issue entitled: Transcription by Odd Pols.


► Facilitated recycling forces Pol III to reinitiate transcription on the same gene
► The macromolecular interactions underlying Pol III recycling are being unveiled.
► Fast Pol III reinitiation is essential for producing abundant Pol III transcripts.
► Facilitated Pol III recycling might be a key target in cell growth regulation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms - Volume 1829, Issues 3–4, March–April 2013, Pages 331–341
نویسندگان
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