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Heritability and Transcriptional Impact of JAK3, STAT5A and STAT6 Variants in a Tyrolean Family

Lee, Hye Kyung; Haikarainen, Teemu; Caf, Yasemin; Furth, Priscilla A.; Knabl, Ludwig; Silvennoinen, Olli; Hennighausen, Lothar (2026-01)

 
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Heritability_and_Transcriptional_Impact_of_JAK3_STAT5A_and_STAT6_Variants_in_a_Tyrolean_Family.pdf (2.554Mt)
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URI
https://urn.fi/URN:NBN:fi:tuni-202602092382


Lee, Hye Kyung
Haikarainen, Teemu
Caf, Yasemin
Furth, Priscilla A.
Knabl, Ludwig
Silvennoinen, Olli
Hennighausen, Lothar
01 / 2026

International Journal of Molecular Sciences
913
doi:10.3390/ijms27020913
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https://urn.fi/URN:NBN:fi:tuni-202602092382

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Peer reviewed
Tiivistelmä
The Janus Kinase (JAK) and Signal Transducers and Activators of Transcription (STAT) pathways regulate a range of biological processes, including immune response and hematopoiesis. While a major research focus has been on somatic human mutations in disease, less is known about the heritability of germline variants and their physiological impact. This study addresses an important issue in population genetics: the context-dependent effects and incomplete penetrance of rare genetic variants in immune pathways. Here we identify the rare JAK3P151R, JAK3R925S, STAT5AV494L, and STAT6Q633H variants in an extended family spanning three generations, integrate in silico analyses and AlphaFold 3 structural predictions, and investigate the immune transcriptomes in probands carrying one or more variants. All four variants are inherited through the germline without any evident clinical or physiological manifestations in the carriers. As individual variants, not all persons carrying a specific variant showed the same immune transcriptome. The presence of activated basal transcriptomes was limited to some, but not all, individuals carrying the above variants. A next step in understanding the role of germline variants will be to understand how and why other factors, including both other germline variants and environmental and developmental factors, influence the likelihood of expression of an activated basal transcriptome.
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Kalevantie 5
PL 617
33014 Tampereen yliopisto
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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste