Smirnov A V, Shnaider T А, Korablev A N, Yunusova A M, Serova I A, Battulin N R
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia Novosibirsk State University, Novosibirsk, Russia.
Vavilovskii Zhurnal Genet Selektsii. 2021 May;25(3):331-336. doi: 10.18699/VJ21.036.
Caseins are major milk proteins that have an evolutionarily conserved role in nutrition. Sequence variations in the casein genes affect milk composition in livestock species. Regulatory elements of the casein genes could be used to direct the expression of desired transgenes into the milk of transgenic animals. Dozens of casein alleles have been identified for goats, cows, sheep, camels and horses, and these sequence variants are associated with altered gene expression and milk protein content. Most of the known mutations affecting casein genes' expression are located in the promoter and 3'-untranslated regions. We performed pronuclear microinjections with Cas9 mRNA and sgRNA against the first coding exon of the mouse Csn1s1 gene to introduce random mutations in the α-casein (Csn1s1) signal peptide sequence at the beginning of the mouse gene. Sanger sequencing of the founder mice identified 40 mutations. As expected, mutations clustered around the sgRNA cut site (3 bp from PAM). Most of the mutations represented small deletions (1-10 bp), but we detected several larger deletions as well (100-300 bp). Functionally most mutations led to gene knockout due to a frameshift or a start codon loss. Some of the mutations represented in-frame indels in the first coding exon. Of these, we describe a novel hypomorphic Csn1s1 (Csn1s1c.4-5insTCC) allele. We measured Csn1s1 protein levels and confirmed that the mutation has a negative effect on milk composition, which shows a 50 % reduction in gene expression and a 40-80 % decrease in Csn1s1 protein amount, compared to the wild-type allele. We assumed that mutation affected transcript stability or splicing by an unknown mechanism. This mutation can potentially serve as a genetic marker for low Csn1s1 expression.
酪蛋白是主要的乳蛋白,在营养方面具有进化上保守的作用。酪蛋白基因的序列变异会影响家畜物种的乳汁成分。酪蛋白基因的调控元件可用于将所需转基因的表达导向转基因动物的乳汁中。已经在山羊、奶牛、绵羊、骆驼和马中鉴定出数十种酪蛋白等位基因,这些序列变异与基因表达改变和乳蛋白含量相关。大多数影响酪蛋白基因表达的已知突变位于启动子和3'非翻译区。我们用针对小鼠Csn1s1基因第一个编码外显子的Cas9 mRNA和sgRNA进行原核显微注射,以在小鼠基因起始处的α-酪蛋白(Csn1s1)信号肽序列中引入随机突变。对奠基小鼠进行桑格测序鉴定出40个突变。正如预期的那样,突变聚集在sgRNA切割位点周围(距PAM 3 bp)。大多数突变代表小缺失(1 - 10 bp),但我们也检测到了一些较大的缺失(100 - 300 bp)。在功能上,大多数突变由于移码或起始密码子丢失导致基因敲除。其中一些突变代表第一个编码外显子中的框内插入缺失。在这些突变中,我们描述了一种新的低表达Csn1s1(Csn1s1c.4 - 5insTCC)等位基因。我们测量了Csn1s1蛋白水平,并证实该突变对乳汁成分有负面影响,与野生型等位基因相比,基因表达降低了50%,Csn1s1蛋白量减少了40 - 80%。我们推测该突变通过未知机制影响转录稳定性或剪接。这种突变有可能作为低Csn1s1表达的遗传标记。