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首页> 外文期刊>Genes, Chromosomes and Cancer >Corrections for mRNA extraction and sample normalization errors find increased mRNA levels may compensate for cancer haplo-insufficiency
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Corrections for mRNA extraction and sample normalization errors find increased mRNA levels may compensate for cancer haplo-insufficiency

机译:对mRNA提取和样品归一化错误的校正发现增加的mRNA水平可能弥补了癌症的单倍型不足

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摘要

The relative mRNA levels of differentially expressed (DE) and housekeeping (HK) genes of six aneuploid cancer lines with large-scale genomic changes identified by SNP/SKY analysis were compared with similar genes in diploid cells. The aneuploid cancer lines had heterogeneous genomic landscapes with subdiploid, diploid, and supradiploid regions and higher overall gene copy numbers compared with diploid cells. The mRNA levels of the haploid, diploid, and triploid HK genes were found to be higher after correction of easily identifiable mRNA measurement errors. Surprisingly, diploid and aneuploid HK gene mRNA levels were the same by standard expression array analyses, despite the higher copy numbers of the cancer cell HK genes. This paradoxical result proved to be due to inaccurate inputs of true intra-cellular mRNAs for analysis. These errors were corrected by analyzing the expression intensities of DE and HK genes in mRNAs extracted from equal cell numbers (50:50) of intact cancer cell and lymphocyte mixtures. Correction for both mRNA extraction/sample normalization errors and total gene copy numbers found the SUIT-2 and PC-3 cell lines' cancer genes both had ~50% higher mRNA levels per single allele than lymphocyte gene alleles. These increased mRNA levels for single transcribed cancer alleles may restore functional mRNA levels to cancer genes rendered haplo-insufficient by the genetic instability of cancer.
机译:将通过SNP / SKY分析鉴定的六种具有大规模基因组变化的非整倍体癌症系的差异表达(DE)和管家(HK)基因的相对mRNA水平与二倍体细胞中的相似基因进行了比较。与二倍体细胞相比,非整倍体癌症系具有具有亚二倍体,二倍体和超倍体区域的异质基因组景观,并且具有更高的整体基因拷贝数。在校正易于识别的mRNA测量误差后,发现单倍体,二倍体和三倍体HK基因的mRNA水平较高。令人惊讶地,尽管癌细胞HK基因的拷贝数更高,但是通过标准表达阵列分析,二倍体和非整倍体HK基因mRNA水平是相同的。事实证明,这种矛盾的结果是由于用于分析的真实细胞内mRNA的输入不正确。通过分析从完整的癌细胞和淋巴细胞混合物的相等细胞数(50:50)提取的mRNA中DE和HK基因的表达强度,可以纠正这些错误。对mRNA提取/样品归一化错误和总基因拷贝数进行校正,发现SUIT-2和PC-3细胞系的癌基因每个单等位基因的mRNA水平均比淋巴细胞基因等位基因高约50%。对于单个转录的癌症等位基因而言,这些增加的mRNA水平可将功能性mRNA水平恢复至因癌症的遗传不稳定而导致单倍不足的癌症基因。

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