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日本纯合缺失的发生率:引物与序列的交叉反应导致实时PCR筛查出现假阴性

Incidence of Homozygous Deletion in Japan: Cross-Reactivity of Primers with Sequence Causes False Negatives in Real-Time PCR Screening.

作者信息

Sakima Makoto, Bouike Yoshihiro, Wada Shin-Ichi, Nakamae Masami, Noguchi Yoriko, Bo Ryosuke, Awano Hiroyuki, Oba Jumpei, Nishio Hisahide

机构信息

Faculty of Nutrition, Kobe Gakuin University, 518 Arise, Ikawadani-cho, Nishi-ku, Kobe 651-2180, Japan.

Department of Clinical Laboratory, Kobe University Hospital, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.

出版信息

Genes (Basel). 2025 Jun 16;16(6):712. doi: 10.3390/genes16060712.

Abstract

: and are causative and modifier genes, respectively, for spinal muscular atrophy (SMA). The incidence of homozygous deletion in Japan is 1 in 20,000. However, the incidence of homozygous deletion in Japan remains unknown. : To clarify the incidence of homozygous deletion in Japan, real-time polymerase chain reaction (PCR) was performed on dried blood spot (DBS) samples collected from newborns nationwide. Samples with positive or ambiguous results were retested using PCR-restriction fragment length polymorphism (PCR-RFLP) and nucleotide sequence analysis. : Of the 1000 DBS samples that were screened using real-time PCR, 51 were positive. Retesting using PCR-RFLP analysis identified 10 false results: six false positives and four false negatives. Therefore, there were 49 true positives among the 1000 samples. Notably, nucleotide sequence analysis revealed that the false negatives were caused by the cross-reactivity of primers with sequences. : The incidence of homozygous deletion in Japan is approximately 1 in 20 people. This incidence is much higher than that of homozygous deletion and may reflect the vulnerability of the region. Importantly, the results of the present study suggest that false negatives in the screening process were caused by cross-reactivity with non-target gene sequences.

摘要

和分别是脊髓性肌萎缩症(SMA)的致病基因和修饰基因。在日本,纯合缺失的发生率为两万分之一。然而,在日本,纯合缺失的发生率仍然未知。为了明确日本纯合缺失的发生率,对从全国新生儿采集的干血斑(DBS)样本进行了实时聚合酶链反应(PCR)。对结果为阳性或不明确的样本,使用PCR-限制性片段长度多态性(PCR-RFLP)和核苷酸序列分析进行重新检测。在使用实时PCR筛选的1000份DBS样本中,51份为阳性。使用PCR-RFLP分析重新检测发现10个假结果:6个假阳性和4个假阴性。因此,在1000个样本中有49个真阳性。值得注意的是,核苷酸序列分析显示,假阴性是由引物与序列的交叉反应引起的。在日本,纯合缺失的发生率约为二十分之一。这一发生率远高于纯合缺失的发生率,可能反映了区域的易损性。重要的是,本研究结果表明,筛查过程中的假阴性是由与非靶基因序列的交叉反应引起的。

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