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含有缬氨酰(Val)的蛋白(VCP)的杂合突变与 VCP 抑制剂的耐药性。

Heterozygous mutations in valosin-containing protein (VCP) and resistance to VCP inhibitors.

机构信息

Department of Laboratory Medicine, University of California San Francisco, 185 Berry Street, San Francisco, 94143, California, USA.

Division of Molecular Medicine, University of New Mexico Health Sciences Center, 915 Camino de Salud NE, Albuquerque, 87131, New Mexico, USA.

出版信息

Sci Rep. 2019 Jul 29;9(1):11002. doi: 10.1038/s41598-019-47085-9.

Abstract

In recent years, multiple studies including ours have reported on the mechanism of resistance towards valosin-containing protein (VCP) inhibitors. While all these studies reported target alterations via mutations in VCP as the primary mechanism of resistance, discrepancies persist to date regarding the zygosity of these mutations responsible for the resistance. In addition, the extent to which resistant cells harbor additional mutations in other genes is not well described. In this study, we performed global transcript analysis of the parental and previously reported VCP inhibitor (CB-5083) resistant cells and found additional mutations in the resistant cells. However, our CRISPR-Cas9 gene editing studies indicate that specific mutations in VCP are sufficient to produce resistance to CB-5083 suggesting the importance of on-target mutations in VCP for resistance. Strikingly, our analysis indicates a preexisting heterozygous frameshift mutation at codon 616 (N616fs*) in one of the VCP alleles in HCT116 cells, and we showed that this mutant allele is subjected to the nonsense-mediated decay (NMD). Accordingly, we identified a heterozygous mutation at codon 526 (L526S) in genomic DNA sequencing but a homozygous L526S mutation in complementary DNA sequencing in our independently generated CB-5083 resistant HCT116 cells, implying that the L526S mutation occurs in the allele that does not harbor the frameshift N616fs* mutation. Our results suggest the NMD as a possible mechanism for achieving the homozygosity of VCP mutant responsible for the resistance to VCP inhibitors while resolving the discrepancies among previous studies. Our results also underscore the importance of performing simultaneous genomic and complementary DNA sequencing when attributing mutational effects on the functionality particularly for an oligomer protein like VCP.

摘要

近年来,包括我们在内的多项研究报告了泛素结合酶 E2 家族成员 5(UBE2F)抑制剂的耐药机制。虽然所有这些研究都报告了靶标改变,即 VCP 突变是耐药的主要机制,但迄今为止,这些导致耐药的突变的杂合性仍存在差异。此外,耐药细胞中其他基因额外突变的程度也没有很好地描述。在这项研究中,我们对亲本细胞和先前报道的 VCP 抑制剂(CB-5083)耐药细胞进行了全转录组分析,发现耐药细胞中存在额外的突变。然而,我们的 CRISPR-Cas9 基因编辑研究表明,VCP 中的特定突变足以产生对 CB-5083 的耐药性,这表明 VCP 中的靶标突变在耐药性中很重要。引人注目的是,我们的分析表明在 HCT116 细胞中的一个 VCP 等位基因中,616 密码子(N616fs*)存在预先存在的杂合移码突变,并且我们表明该突变等位基因受到无意义介导的衰变(NMD)的影响。因此,我们在独立生成的 CB-5083 耐药 HCT116 细胞的基因组 DNA 测序中鉴定出 526 密码子(L526S)的杂合突变,但在互补 DNA 测序中鉴定出 526 密码子(L526S)的纯合突变,这意味着 L526S 突变发生在不携带移码 N616fs*突变的等位基因中。我们的结果表明,NMD 可能是一种机制,可以实现对导致 VCP 抑制剂耐药的 VCP 突变体的纯合性,同时解决先前研究之间的差异。我们的结果还强调了在归因于功能突变时,特别是对于像 VCP 这样的寡聚蛋白,同时进行基因组和互补 DNA 测序的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ccc/6662852/52f06a288dd3/41598_2019_47085_Fig1_HTML.jpg

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