TY - JOUR
T1 - 2D gel electrophoresis reveals dynamics of t-loop formation during the cell cycle and t-loop in maintenance regulated by heterochromatin state
AU - Zhang, Zepeng
AU - Zhang, Tianpeng
AU - Ge, Yuanlong
AU - Tang, Mengfan
AU - Ma, Wenbin
AU - Zhang, Qinfen
AU - Gong, Shengzhao
AU - Wright, Woodring E
AU - Shay, Jerry
AU - Liu, Haiying
AU - Zhao, Yong
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China Grants 81771506, 31571410, and 31701196, National Key R&D Pro-gram of China Grant 2018YFA0107000, and Guangzhou Municipal People’s Livelihood Science and Technology Plan Grants 201803010108 and 201604016111. The authors declare that they have no conflicts of interest with the contents of this article.
Publisher Copyright:
© 2019 Zhang et al.
PY - 2019/4/19
Y1 - 2019/4/19
N2 - Linear chromosome ends are capped by telomeres that have been previously reported to adopt a t-loop structure. The lack of simple methods for detecting t-loops has hindered progress in understanding the dynamics of t-loop formation and its function in protecting chromosome ends. Here, we employed a classical two-dimensional agarose gel method (2D gel method) to innovatively apply to t-loop detection. Briefly, restriction fragments of genomic DNA were separated in a 2D gel, and the telomere sequence was detected by in-gel hybridization with telomeric probe. Using this method, we found that t-loops are present throughout the cell cycle, and t-loop formation tightly couples to telomere replication. We also observed that t-loop abundance positively correlates with chromatin condensation, i.e. cells with less compact telomeric chromatin (ALT cells and trichostatin A (TSA)-treated HeLa cells) exhibited fewer t-loops. Moreover, we observed that telomere dysfunction-induced foci, ALT-associated promyelocytic leukemia bodies, and telomere sister chromatid exchanges are activated upon TSAinduced loss of t-loops. These findings confirm the importance of the t-loop in protecting linear chromosomes from damage or illegitimate recombination.
AB - Linear chromosome ends are capped by telomeres that have been previously reported to adopt a t-loop structure. The lack of simple methods for detecting t-loops has hindered progress in understanding the dynamics of t-loop formation and its function in protecting chromosome ends. Here, we employed a classical two-dimensional agarose gel method (2D gel method) to innovatively apply to t-loop detection. Briefly, restriction fragments of genomic DNA were separated in a 2D gel, and the telomere sequence was detected by in-gel hybridization with telomeric probe. Using this method, we found that t-loops are present throughout the cell cycle, and t-loop formation tightly couples to telomere replication. We also observed that t-loop abundance positively correlates with chromatin condensation, i.e. cells with less compact telomeric chromatin (ALT cells and trichostatin A (TSA)-treated HeLa cells) exhibited fewer t-loops. Moreover, we observed that telomere dysfunction-induced foci, ALT-associated promyelocytic leukemia bodies, and telomere sister chromatid exchanges are activated upon TSAinduced loss of t-loops. These findings confirm the importance of the t-loop in protecting linear chromosomes from damage or illegitimate recombination.
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U2 - 10.1074/jbc.RA119.007677
DO - 10.1074/jbc.RA119.007677
M3 - Article
C2 - 30819801
AN - SCOPUS:85064855639
SN - 0021-9258
VL - 294
SP - 6645
EP - 6656
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 16
ER -