Evidence map›Paper›PMID 39891056›Full record

ArticleBMC molecular and cell biology2025

Assessment of XCI skewing and demonstration of XCI escape region based on single-cell RNA sequencing: comparison between female Grave's disease and control.

In-Cheol Baek, Soo Yeun Sim, Byung-Kyu Suh, Tai-Gyu Kim, Won Kyoung Cho

Abstract readComparative Study
In one paragraph

Article in BMC molecular and cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

In-Cheol BaekCatholic Hematopoietic Stem Cell Bank, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-3630-3364
Soo Yeun SimDepartment of Pediatrics, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-4221-6080
Byung-Kyu SuhDepartment of Pediatrics, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-1971-0232
Tai-Gyu KimDepartment of Microbiology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-2226-2138
Won Kyoung ChoDepartment of Pediatrics, College of Medicine, St. Vincent's Hospital, The Catholic University of Korea, 93, Jungbu-daero, Paldal-gu, Suwon-si, Seoul, Gyeonggi-do, 16247, Republic of Korea. wendy626@catholic.ac.kr.ORCID https://orcid.org/0000-0003-0918-0565

Funding

National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (2022R1F1A1062761) 2022R1F1A1062761
6 · The paper itself

Abstract

backgroundThe reactivation and loss of mosaicism hypothesis due to X chromosome inactivation (XCI) skewing and escape could influence gender differences in autoimmune diseases. XCI selectively inactivates one of the two X chromosomes in females.

methodsTo estimate XCI skewing and the occurrence of XCI escape, we conducted a normal female (NF) without a history of autoimmune thyroid disease (AITD) and a patient with Grave's disease (GD) based on a thyroid diagnosis. After single-cell RNA sequencing, heterozygous variants were converted and transformed. XCI skewing was calculated using the formula and the skewing degree was defined. NF/GD genes were compared using correction methods. Positions are heterozygous within a single cell as indicated by a unique barcode.

resultsXCI skewing showed 45.8%/48.9% relatively random, 29.4%/27.0% skewing, 24.6%/23.7% severe skewing, and 0.2%/0.4% extreme severe skewing. 24.8%/24.1% in NF/GD exhibited severe skewing or higher. A total of 13 genes were significantly associated with XCI skewing ratios in NF/GD cells. In total, 371/250 nucleotide positions with only one barcode (representing a unique cell) were identified for XCI escape. A total of 143/52 nucleotide positions spanned 20/6 genes, and 12/1 genes were identified as XCI escapes.

conclusionsThese results could aid in understanding the immunogenetics of gender differences in various autoimmune disease pathophysiologies.

Indexed as

Chromosomes, Human, XGraves DiseaseX Chromosome InactivationAdultCase-Control StudiesFemaleHumansSequence Analysis, RNASingle-Cell AnalysisAutoimmune thyroid diseaseSingle-cell RNA sequencingSingle nucleotide polymorphismX chromosome inactivationXCI skewing and escape

Identifiers

PMID39891056
PMCPMC11786500

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