Tissue-specific reduction in MLH1 expression induces microsatellite instability in intestine of Mlh1+/- mice

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Shrestha , K , Aska , E , Tuominen , M & Kauppi , L 2021 , ' Tissue-specific reduction in MLH1 expression induces microsatellite instability in intestine of Mlh1+/- mice ' , DNA Repair , vol. 106 . https://doi.org/10.1016/j.dnarep.2021.103178

Title: Tissue-specific reduction in MLH1 expression induces microsatellite instability in intestine of Mlh1+/- mice
Author: Shrestha, Kul; Aska, Elli; Tuominen, Minna; Kauppi, Liisa
Contributor: University of Helsinki, Research Programs Unit
University of Helsinki, Research Program in Systems Oncology
University of Helsinki, Institute for Molecular Medicine Finland
University of Helsinki, Medicum
Date: 2021-07-09
Language: eng
Number of pages: 10
Belongs to series: DNA Repair
ISSN: 1568-7864
URI: http://hdl.handle.net/10138/333506
Abstract: Tumors of Lynch syndrome (LS) patients display high levels of microsatellite instability (MSI), which results from complete loss of DNA mismatch repair (MMR), in line with Knudson’s two-hit hypothesis. Why some organs, in particular those of the gastrointestinal (GI) tract, are prone to tumorigenesis in LS remains unknown. We hypothesized that MMR is haploinsufficient in certain tissues, compromising microsatellite stability in a tissue-specific manner before tumorigenesis. Using mouse genetics, we tested how levels of MLH1, a central MMR protein, affect age- and tissue-specific microsatellite stability in vivo and whether elevated MSI is detectable prior to loss of MMR function and to neoplastic growth. To assess putative tissue-specific MMR haploinsufficiency, we determined relevant molecular phenotypes (MSI, Mlh1 promoter methylation status, MLH1 protein and RNA levels) in jejuna of Mlh1+/− mice and compared them to those in spleen, as well as to MMR-proficient and -deficient controls (Mlh1+/+ and Mlh1−/− mice). While spleen MLH1 levels of Mlh1+/− mice were, as expected, approximately 50 % compared to wildtype mice, MLH1 levels in jejunum varied substantially between individual Mlh1+/− mice and moreover, decreased with age. Mlh1+/− mice with soma-wide Mlh1 promoter methylation often displayed severe MLH1 depletion in jejunum. Reduced (but still detectable) MLH1 levels correlated with elevated MSI in Mlh1+/− jejunum. MSI in jejunum increased with age, while in spleens of the same mice, MLH1 levels and microsatellites remained stable. Thus, MLH1 expression levels are particularly labile in intestine of Mlh1+/− mice, giving rise to tissue-specific MSI long before neoplasia. A similar mechanism likely also operates also in the human GI epithelium and could explain the wide range in age-of-onset of LS-associated tumorigenesis.
Subject: 1184 Genetics, developmental biology, physiology
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