[HTML][HTML] High resolution size analysis of fetal DNA in the urine of pregnant women by paired-end massively parallel sequencing

NBY Tsui, P Jiang, KCK Chow, X Su, TY Leung, H Sun… - PloS one, 2012 - journals.plos.org
NBY Tsui, P Jiang, KCK Chow, X Su, TY Leung, H Sun, KCA Chan, RWK Chiu, YMD Lo
PloS one, 2012journals.plos.org
Background Fetal DNA in maternal urine, if present, would be a valuable source of fetal
genetic material for noninvasive prenatal diagnosis. However, the existence of fetal DNA in
maternal urine has remained controversial. The issue is due to the lack of appropriate
technology to robustly detect the potentially highly degraded fetal DNA in maternal urine.
Methodology We have used massively parallel paired-end sequencing to investigate cell-
free DNA molecules in maternal urine. Catheterized urine samples were collected from …
Background
Fetal DNA in maternal urine, if present, would be a valuable source of fetal genetic material for noninvasive prenatal diagnosis. However, the existence of fetal DNA in maternal urine has remained controversial. The issue is due to the lack of appropriate technology to robustly detect the potentially highly degraded fetal DNA in maternal urine.
Methodology
We have used massively parallel paired-end sequencing to investigate cell-free DNA molecules in maternal urine. Catheterized urine samples were collected from seven pregnant women during the third trimester of pregnancies. We detected fetal DNA by identifying sequenced reads that contained fetal-specific alleles of the single nucleotide polymorphisms. The sizes of individual urinary DNA fragments were deduced from the alignment positions of the paired reads. We measured the fractional fetal DNA concentration as well as the size distributions of fetal and maternal DNA in maternal urine.
Principal Findings
Cell-free fetal DNA was detected in five of the seven maternal urine samples, with the fractional fetal DNA concentrations ranged from 1.92% to 4.73%. Fetal DNA became undetectable in maternal urine after delivery. The total urinary cell-free DNA molecules were less intact when compared with plasma DNA. Urinary fetal DNA fragments were very short, and the most dominant fetal sequences were between 29 bp and 45 bp in length.
Conclusions
With the use of massively parallel sequencing, we have confirmed the existence of transrenal fetal DNA in maternal urine, and have shown that urinary fetal DNA was heavily degraded.
PLOS