Modeling X chromosome inactivation using t5iLA naive human pluripotent stem cells

被引:0
作者
Shang, Yudan [1 ]
Wang, Nannan [2 ,3 ,4 ]
Wang, Haoyi [2 ,3 ,4 ,5 ]
An, Chenrui [1 ]
Sun, Wen [2 ,3 ,5 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 3, Guangdong Prov Clin Res Ctr Obstet & Gynecol, Guangdong Hong Kong Macao Greater Bay Area Higher, Guangzhou, Peoples R China
[2] Chinese Acad Sci, State Key Lab Stem Cell & Reprod Biol, Inst Zool, Beijing, Peoples R China
[3] Chinese Acad Sci, Inst Stem Cell & Regenerat, Beijing, Peoples R China
[4] Univ Chinese Acad Sci, Beijing, Peoples R China
[5] Beijing Inst Stem Cell & Regenerat Med, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
X chromosome inactivation; Human embryonic stem cells; Early embryogenesis; H3; LYSINE-27; METHYLATION; HISTONE H2A; ESTABLISHMENT; RECRUITMENT; PROTEINS;
D O I
10.1186/s12915-024-01994-y
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background X chromosome inactivation (XCI) is a critical epigenetic event for dosage compensation of X-linked genes in female mammals, ensuring developmental stability. A robust in vitro model is required for mimicking XCI during the early stages of embryonic development. This methodology article introduces an advanced framework for the in-depth study of XCI using human pluripotent stem cells (hPSCs). By focusing on the transition between naive and primed pluripotent states, we highlight the role of long non-coding RNA X-inactive specific transcript (XIST) and epigenetic alterations in mediating XCI. Results Our methodology enables the distinction between naive and primed hESCs based on XIST expression and the activity of X-linked reporters, facilitating the investigation of XCI initiation and maintenance. Through detailed experimental procedures, we demonstrate the utility of our hESC lines in modeling the process of human XCI, including the establishment of conditions for random XCI induction and the analysis of X chromosome reactivation. Methods The study outlines a comprehensive approach for characterizing the X chromosome status in hPSCs, employing dual fluorescent reporter hESC lines. These reporter lines enable real-time tracking of XCI dynamics through differentiation processes. We detailed protocols for the induction of X chromosome reactivation and inactivation, as well as the X status characterization methods including cultivation of hESCs, flow cytometric analysis, RNA fluorescence in situ hybridization (FISH), and transcriptome sequencing, providing a step-by-step guide for researchers to investigate XCI mechanisms in vitro. Conclusions This article provides a detailed, reproducible methodology for studying XCI mechanisms in vitro, employing hPSCs as a model system. It presents a significant advance in our ability to investigate XCI, offering potential applications in developmental biology, disease modeling, and regenerative medicine. By facilitating the study of XCI dynamics, this methodological framework paves the way for deeper understanding and manipulation of this fundamental biological process.
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页数:12
相关论文
共 44 条
[21]   Live imaging of X chromosome reactivation dynamics in early mouse development can discriminate naive from primed pluripotent stem cells [J].
Kobayashi, Shin ;
Hosoi, Yusuke ;
Shiura, Hirosuke ;
Yamagata, Kazuo ;
Takahashi, Saori ;
Fujihara, Yoshitaka ;
Kohda, Takashi ;
Okabe, Masaru ;
Ishino, Fumitoshi .
DEVELOPMENT, 2016, 143 (16) :2958-2964
[22]   X-Inactivation, Imprinting, and Long Noncoding RNAs in Health and Disease [J].
Lee, Jeannie T. ;
Bartolomei, Marisa S. .
CELL, 2013, 152 (06) :1308-1323
[23]   Derivation of Pre-X Inactivation Human Embryonic Stem Cells under Physiological Oxygen Concentrations [J].
Lengner, Christopher J. ;
Gimelbrant, Alexander A. ;
Erwin, Jennifer A. ;
Cheng, Albert Wu ;
Guenther, Matthew G. ;
Welstead, G. Grant ;
Alagappan, Raaji ;
Frampton, Garrett M. ;
Xu, Ping ;
Muffat, Julien ;
Santagata, Sandro ;
Powers, Doug ;
Barrett, C. Brent ;
Young, Richard A. ;
Lee, Jeannie T. ;
Jaenisch, Rudolf ;
Mitalipova, Maisam .
CELL, 2010, 141 (05) :872-883
[24]   X Chromosome Inactivation and Epigenetic Responses to Cellular Reprogramming [J].
Lessing, Derek ;
Anguera, Montserrat C. ;
Lee, Jeannie T. .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 14, 2013, 14 :85-110
[25]   Two-Step Imprinted X Inactivation: Repeat versus Genic Silencing in the Mouse [J].
Namekawa, Satoshi H. ;
Payer, Bernhard ;
Huynh, Khanh D. ;
Jaenisch, Rudolf ;
Lee, Jeannie T. .
MOLECULAR AND CELLULAR BIOLOGY, 2010, 30 (13) :3187-3205
[26]   Recurrent Variations in DNA Methylation in Human Pluripotent Stem Cells and Their Differentiated Derivatives [J].
Nazor, Kristopher L. ;
Altun, Gulsah ;
Lynch, Candace ;
Tran, Ha ;
Harness, Julie V. ;
Slavin, Ileana ;
Garitaonandia, Ibon ;
Mueller, Franz-Josef ;
Wang, Yu-Chieh ;
Boscolo, Francesca S. ;
Fakunle, Eyitayo ;
Dumevska, Biljana ;
Lee, Sunray ;
Park, Hyun Sook ;
Olee, Tsaiwei ;
D'Lima, Darryl D. ;
Semechkin, Ruslan ;
Parast, Mana M. ;
Galat, Vasiliy ;
Laslett, Andrew L. ;
Schmidt, Uli ;
Keirstead, Hans S. ;
Loring, Jeanne F. ;
Laurent, Louise C. .
CELL STEM CELL, 2012, 10 (05) :620-634
[27]   Eutherian mammals use diverse strategies to initiate X-chromosome inactivation during development [J].
Okamoto, Ikuhiro ;
Patrat, Catherine ;
Thepot, Dominique ;
Peynot, Nathalie ;
Fauque, Patricia ;
Daniel, Nathalie ;
Diabangouaya, Patricia ;
Wolf, Jean-Philippe ;
Renard, Jean-Paul ;
Duranthon, Veronique ;
Heard, Edith .
NATURE, 2011, 472 (7343) :370-U141
[28]   Human Embryonic Stem Cells Do Not Change Their X Inactivation Status during Differentiation [J].
Patel, Sanjeet ;
Bonora, Giancarlo ;
Sahakyan, Anna ;
Kim, Rachel ;
Chronis, Constantinos ;
Langerman, Justin ;
Fitz-Gibbon, Sorel ;
Rubbi, Liudmilla ;
Skelton, Rhys J. P. ;
Ardehali, Reza ;
Pellegrini, Matteo ;
Lowry, William E. ;
Clark, Amander T. ;
Plath, Kathrin .
CELL REPORTS, 2017, 18 (01) :54-67
[29]   X chromosome inactivation in human development [J].
Patrat, Catherine ;
Ouimette, Jean-Francois ;
Rougeulle, Claire .
DEVELOPMENT, 2020, 147 (01)
[30]  
Petropoulos S, 2016, CELL, V167, P285, DOI [10.1016/j.cell.2016.08.009, 10.1016/j.cell.2016.03.023]