Tsitsikov Erdyni N, Phan Khanh P, Liu Yufeng, Tsytsykova Alla V, Paterno Rosalia, Sherry David M, Johnson Anthony C, Dunn Ian F
Department of Neurosurgery, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States of America.
Neuroscience Ph.D. Program, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States of America.
PLoS One. 2024 Dec 4;19(12):e0290487. doi: 10.1371/journal.pone.0290487. eCollection 2024.
Here, we describe a spontaneous mouse mutant with a deletion in a predicted gene 2310061I04Rik (Rik) of unknown function located on chromosome 17. A 59 base pair long deletion occurred in the first intron of the Rik gene and disrupted its expression. Riknull mice were born healthy and appeared anatomically normal up to two weeks of age. After that, these mice showed inhibited growth, ataxic gait, and died shortly after postnatal day 24 (P24). Transcriptome analysis at P14 and P23 revealed significantly reduced expression of mitochondrial genes in Riknull brains compared to wild type controls including mt-Nd4, mt-Cytb, mt-Nd2, mt-Co1, mt-Atp6, and others. Similarly, genes specific for myelinating oligodendrocytes also showed reduced expression in P23 Riknull brains compared to controls. Histological examination of anterior thalamic nuclei demonstrated decreased myelination of anteroventral nuclei but not of anterodorsal nuclei in P23 Riknull mice. Myelination of the anterior commissure was also impaired and displayed extensive vacuolation. Consistently with these findings, immunohistochemistry showed reduced expression of Opalin, a glycoprotein expressed in differentiated oligodendrocytes. Taken together, these results suggest that RIK is important for oligodendrocyte maturation and myelination in the developing brain.
在此,我们描述了一种自发的小鼠突变体,其位于17号染色体上的一个功能未知的预测基因2310061I04Rik(Rik)存在缺失。一个59个碱基对长的缺失发生在Rik基因的第一个内含子中,并破坏了其表达。Rik基因敲除小鼠出生时健康,在两周龄前解剖结构看起来正常。在此之后,这些小鼠生长受到抑制,步态共济失调,并在出生后第24天(P24)后不久死亡。在P14和P23进行的转录组分析显示,与野生型对照相比,Rik基因敲除小鼠大脑中的线粒体基因表达显著降低,包括mt-Nd4、mt-Cytb、mt-Nd2、mt-Co1、mt-Atp6等。同样,与对照相比,在P23的Rik基因敲除小鼠大脑中,髓鞘形成少突胶质细胞特异性基因的表达也降低。对丘脑前核的组织学检查表明,P23的Rik基因敲除小鼠前腹侧核的髓鞘形成减少,但前背侧核未减少。前连合的髓鞘形成也受损,并表现出广泛的空泡化。与这些发现一致,免疫组织化学显示在分化的少突胶质细胞中表达的糖蛋白Opalin的表达减少。综上所述,这些结果表明RIK对发育中大脑的少突胶质细胞成熟和髓鞘形成很重要。