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tRNA Genes Affect Chromosome Structure and Function via Local Effects
Author(s) -
Omar Hamdani,
Namrita Dhillon,
Tsung-Han S. Hsieh,
Takahiro Fujita,
Josefina Ocampo,
Jacob G. Kirkland,
Josh Lawrimore,
Tetsuya Kobayashi,
Barbara Friedman,
Derek Fulton,
Kenneth Wu,
Răzvan V. Chereji,
Masaya Oki,
Kerry Bloom,
David J. Clark,
Oliver J. Rando,
Rohinton T. Kamakaka
Publication year - 2019
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00432-18
Subject(s) - biology , chromatin , heterochromatin , centromere , genetics , chromosome , chromosome conformation capture , nucleosome , gene , genomic organization , genome , computational biology , transcription factor , enhancer
The genome is packaged and organized in an ordered, nonrandom manner, and specific chromatin segments contact nuclear substructures to mediate this organization. tRNA genes (tDNAs) are binding sites for transcription factors and architectural proteins and are thought to play an important role in the organization of the genome. In this study, we investigate the roles of tDNAs in genomic organization and chromosome function by editing a chromosome so that it lacked any tDNAs. Surprisingly our analyses of this tDNA-less chromosome show that loss of tDNAs does not grossly affect chromatin architecture or chromosome tethering and mobility. However, loss of tDNAs affects local nucleosome positioning and the binding of SMC proteins at these loci. The absence of tDNAs also leads to changes in centromere clustering and a reduction in the frequency of long-range HML-HMR heterochromatin clustering with concomitant effects on gene silencing. We propose that the tDNAs primarily affect local chromatin structure, which results in effects on long-range chromosome architecture.

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