Gene expression analysis in pregnant women and their infants identifies unique fetal biomarkers that circulate in maternal blood.

The discovery of fetal mRNA transcripts in the maternal circulation holds great promise for noninvasive prenatal diagnosis. To identify potential fetal biomarkers, we studied whole blood and plasma gene transcripts that were common to 9 term pregnant women and their newborns but absent or reduced in the mothers postpartum. RNA was isolated from peripheral or umbilical blood and hybridized to gene expression arrays. Gene expression, paired Student's t test, and pathway analyses were performed. In whole blood, 157 gene transcripts met statistical significance. These fetal biomarkers included 27 developmental genes, 5 sensory perception genes, and 22 genes involved in neonatal physiology. Transcripts were predominantly expressed or restricted to the fetus, the embryo, or the neonate. Real-time RT-PCR amplification confirmed the presence of specific gene transcripts; SNP analysis demonstrated the presence of 3 fetal transcripts in maternal antepartum blood. Comparison of whole blood and plasma samples from the same pregnant woman suggested that placental genes are more easily detected in plasma. We conclude that fetal and placental mRNA circulates in the blood of pregnant women. Transcriptional analysis of maternal whole blood identifies a unique set of biologically diverse fetal genes and has a multitude of clinical applications.

[1]  Jill L. Maron,et al.  Prenatal diagnosis using cell‐free nucleic acids in maternal body fluids: A decade of progress , 2007, American journal of medical genetics. Part C, Seminars in medical genetics.

[2]  G. Saade,et al.  Labor-Associated Gene Expression in the Human Uterine Fundus, Lower Segment, and Cervix , 2006, PLoS medicine.

[3]  R. Chiu,et al.  Time profile of appearance and disappearance of circulating placenta-derived mRNA in maternal plasma. , 2006, Clinical chemistry.

[4]  Zuhong Lu,et al.  A semi‐quantitative microarray method to detect fetal RNAs in maternal plasma , 2005, Prenatal diagnosis.

[5]  Jean YH Yang,et al.  Bioconductor: open software development for computational biology and bioinformatics , 2004, Genome Biology.

[6]  L. V. Van Eldik,et al.  Increased susceptibility of S100B transgenic mice to perinatal hypoxia‐ischemia , 2004, Annals of neurology.

[7]  K. C. Chan,et al.  Systematic micro-array based identification of placental mRNA in maternal plasma: towards non-invasive prenatal gene expression profiling , 2004, Journal of Medical Genetics.

[8]  Angela Y. Chen,et al.  Circulating Cell‐Free Fetal Nucleic Acid Analysis May Be a Novel Marker of Fetomaternal Hemorrhage after Elective First‐Trimester Termination of Pregnancy , 2004, Annals of the New York Academy of Sciences.

[9]  Brad T. Sherman,et al.  DAVID: Database for Annotation, Visualization, and Integrated Discovery , 2003, Genome Biology.

[10]  A. Benachi,et al.  Fetal expressed gene analysis in maternal blood: a new tool for noninvasive study of the fetus. , 2003, Clinical chemistry.

[11]  R. Chiu,et al.  The concentration of circulating corticotropin-releasing hormone mRNA in maternal plasma is increased in preeclampsia. , 2003, Clinical chemistry.

[12]  R. Chiu,et al.  mRNA of placental origin is readily detectable in maternal plasma , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[13]  P. Khatri,et al.  Global functional profiling of gene expression ? ? This work was funded in part by a Sun Microsystem , 2003 .

[14]  Uwe Oelmueller,et al.  Stabilization of mRNA expression in whole blood samples. , 2002, Clinical chemistry.

[15]  Y. Lo,et al.  Stability of endogenous and added RNA in blood specimens, serum, and plasma. , 2002, Clinical chemistry.

[16]  P. Johnson,et al.  Presence of filterable and nonfilterable mRNA in the plasma of cancer patients and healthy individuals. , 2002, Clinical chemistry.

[17]  L. Poon,et al.  Presence of fetal RNA in maternal plasma. , 2000, Clinical chemistry.

[18]  K. Livak,et al.  Allelic discrimination using fluorogenic probes and the 5' nuclease assay. , 1999, Genetic analysis : biomolecular engineering.

[19]  T K Lau,et al.  Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. , 1998, American journal of human genetics.

[20]  A. Páldi,et al.  Early Recognition of Pregnancy by the Maternal Immune System , 1997, American journal of reproductive immunology.

[21]  G. Weil,et al.  Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[22]  S. Latt,et al.  Isolation of fetal DNA from nucleated erythrocytes in maternal blood. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[23]  J. Eberwine,et al.  Amplified RNA synthesized from limited quantities of heterogeneous cDNA. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[24]  Maqc Consortium The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements , 2006, Nature Biotechnology.

[25]  T Foitzi,et al.  Allelic discrimination using fluorogenic probes and the 5' nuclease assay , 1999 .

[26]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .

[27]  G. Wood,et al.  Is restricted antigen presentation the explanation for fetal allograft survival? , 1994, Immunology today.