Literature DB >> 26782455

Isolation and analysis of cell-free fetal DNA from maternal peripheral blood in Chinese women.

W C Yang1, L Zhu1, Y M Qiu1,2, B X Zhou1, J L Cheng1, C L Wei1,3, H C Chen4, L Y Li5, X D Fu6, J J Fu1,3,6.   

Abstract

Non-invasive prenatal diagnosis is used to detect the genetic material of the fetus by isolating the cell-free fetal DNA (cffDNA) from maternal peripheral blood. In order to establish an isolation method for cffDNA from maternal peripheral blood in Chinese women, the cffDNA was acquired with a two-step centrifugation using a QlAamp DNA Blood mini kit. The SRY gene of plasma DNA was amplified by polymerase chain reaction (PCR). Real-time quantitative PCR was used to measure the concentration of cffDNA in maternal peripheral blood in different pregnant women. The results of the SRY gene amplification of plasma DNA from pregnant women was the same as that of the amniocyte DNA. The average concentration of cffDNA in maternal peripheral blood of pregnant women in different gestational stages was 0.98 ng/mL (0.26-1.49 ng/mL), 1.43 ng/mL (0.46- 2.34 ng/mL), and 1.95 ng/mL (0.65-6.81 ng/mL) from early, middle, and late gestational stages, respectively. The mean of cffDNA from total DNA in plasma in different stages of gestation was 22.28% (9.86-27.81%). The lowest concentration of DNA amplified by nested-PCR in our research was 10-4-10-3 ng/μL. The isolation method for cffDNA from maternal peripheral blood was successfully established and further research into its applications will be conducted.

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Year:  2015        PMID: 26782455     DOI: 10.4238/2015.December.22.34

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  5 in total

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Journal:  Diagnostics (Basel)       Date:  2021-04-28

2.  Diagnosis for choroideremia in a large Chinese pedigree by next‑generation sequencing (NGS) and non‑invasive prenatal testing (NIPT).

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Journal:  Eur J Obstet Gynecol Reprod Biol X       Date:  2019-05-07

4.  Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.

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Journal:  Front Immunol       Date:  2020-12-07       Impact factor: 7.561

5.  Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy.

Authors:  Saber Imani; Jingliang Cheng; Marzieh Dehghan Shasaltaneh; Chunli Wei; Lisha Yang; Shangyi Fu; Hui Zou; Md Asaduzzaman Khan; Xianqin Zhang; Hanchun Chen; Dianzheng Zhang; Chengxia Duan; Hongbin Lv; Yumei Li; Rui Chen; Junjiang Fu
Journal:  Oncotarget       Date:  2017-11-09
  5 in total

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