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Arginine‐ but not alanine‐rich carboxy‐termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti

机译:富含精氨酸而不是富含丙氨酸的羧基末端引发鱼鳞病伴五彩纸屑的突变型角蛋白10的核易位

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摘要

Ichthyosis with confetti (IWC) is a genodermatosis associated with dominant‐negative variants in ( ) or ( ). These frameshift variants result in extended aberrant proteins, localized to the nucleus rather than the cytoplasm. This mislocalization is thought to occur as a result of the altered carboxy (C)‐terminus, from poly‐glycine to either a poly‐arginine or ‐alanine tail. Previous studies on the type of C‐terminus and subcellular localization of the respective mutant protein are divergent. In order to fully elucidate the pathomechanism of IWC, a greater understanding is critical. This study aimed to establish the consequences for localization and intermediate filament formation of altered keratin 10 (K10) C‐termini. To achieve this, plasmids expressing distinct variants were generated. Sequences encoded all possible reading frames of the K10 C‐terminus as well as a nonsense variant. A keratinocyte line was transfected with these plasmids. Additionally, gene editing was utilized to introduce frameshift variants in exon 6 and exon 7 at the endogenous locus. Cellular localization of aberrant K10 was observed via immunofluorescence using various antibodies. In each setting, immunofluorescence analysis demonstrated aberrant nuclear localization of K10 featuring an arginine‐rich C‐terminus. However, this was not observed with K10 featuring an alanine‐rich C‐terminus. Instead, the protein displayed cytoplasmic localization, consistent with wild‐type and truncated forms of K10. This study demonstrates that, of the various 3′ frameshift variants of , exclusively arginine‐rich C‐termini lead to nuclear localization of K10.
机译:五彩纸屑鱼鳞病(IWC)是一种与()或()中显性阴性变体有关的遗传性皮肤病。这些移码变体导致延伸的异常蛋白,定位于细胞核而不是细胞质。这种错位被认为是由于羧基末端的改变,从聚甘氨酸变为聚精氨酸或丙氨酸尾部。先前对C末端类型和相应突变蛋白的亚细胞定位的研究存在分歧。为了充分阐明万国表的致病机理,加深了解是至关重要的。这项研究的目的是确定改变的角蛋白10(K10)C-末端的定位和中间丝形成的后果。为此,产生了表达不同变体的质粒。序列编码了所有可能的K10 C末端阅读框以及无意义的变体。用这些质粒转染角质形成细胞系。另外,利用基因编辑在内源基因座的外显子6和外显子7中引入移码变体。通过使用各种抗体的免疫荧光观察到异常的K10的细胞定位。在每种情况下,免疫荧光分析均显示具有精氨酸富集的C末端的K10异常核定位。但是,使用富含丙氨酸的C末端的K10却没有观察到这一点。相反,该蛋白表现出细胞质定位,与K10的野生型和截短形式一致。这项研究表明,在仅富含精氨酸的C末端的3'移码变体中,K10的核定位。

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