Mod(mdg4) variants repress telomeric retrotransposon HeT-A by blocking subtelomeric enhancers

Author:

Takeuchi Chikara1,Yokoshi Moe2,Kondo Shu3,Shibuya Aoi1,Saito Kuniaki3,Fukaya Takashi24ORCID,Siomi Haruhiko1ORCID,Iwasaki Yuka W156

Affiliation:

1. Department of Molecular Biology, Keio University School of Medicine , Tokyo 160-8582 , Japan

2. Laboratory of Transcription Dynamics, Research Center for Biological Visualization, Institute for Quantitative Biosciences, The University of Tokyo , Tokyo 113-0032 , Japan

3. Department of Chromosome Science, National Institute of Genetics, Research Organization of Information and Systems (ROIS) , Shizuoka 411-8540 , Japan

4. Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo , Tokyo 113-0032 , Japan

5. Laboratory for Functional Non-coding Genomics, RIKEN Center for Integrative Medical Sciences , Yokohama 230-0045 , Japan

6. Japan Science and Technology Agency (JST), Precursory Research for Embryonic Science and Technology (PRESTO) , Saitama 332-0012 , Japan

Abstract

Abstract Telomeres in Drosophila are composed of sequential non-LTR retrotransposons HeT-A, TART and TAHRE. Although they are repressed by the PIWI-piRNA pathway or heterochromatin in the germline, the regulation of these retrotransposons in somatic cells is poorly understood. In this study, we demonstrated that specific splice variants of Mod(mdg4) repress HeT-A by blocking subtelomeric enhancers in ovarian somatic cells. Among the variants, we found that the Mod(mdg4)-N variant represses HeT-A expression the most efficiently. Subtelomeric sequences bound by Mod(mdg4)-N block enhancer activity within subtelomeric TAS-R repeats. This enhancer-blocking activity is increased by the tandem association of Mod(mdg4)-N to repetitive subtelomeric sequences. In addition, the association of Mod(mdg4)-N couples with the recruitment of RNA polymerase II to the subtelomeres, which reinforces its enhancer-blocking function. Our findings provide novel insights into how telomeric retrotransposons are regulated by the specific variants of insulator proteins associated with subtelomeric sequences.

Funder

Japan Science and Technology Agency

Japan Society of the Promotion of Science

Koyo Sakaguchi Memorial Keio University Medical Science Fund

Ushioda Memorial Fund

Sumitomo Foundation

Senri Life Science Foundation

Mitsubishi Foundation

Takeda Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics

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