Systematic Identification of Spontaneous Preterm Birth-Associated RNA Transcripts in Maternal Plasma

Background Spontaneous preterm birth (SPB, before 37 gestational weeks) is a major cause of perinatal mortality and morbidity, but its pathogenesis remains unclear. Studies on SPB have been hampered by the limited availability of markers for SPB in predelivery clinical samples that can be easily compared with gestational age-matched normal controls. We hypothesize that SPB involves aberrant placental RNA expression, and that such RNA transcripts can be detected in predelivery maternal plasma samples, which can be compared with gestational age-matched controls. Principal Findings Using gene expression microarray to profile essentially all human genes, we observed that 426 probe signals were changed by >2.9-fold in the SPB placentas, compared with the spontaneous term birth (STB) placentas. Among the genes represented by those probes, we observed an over-representation of functions in RNA stabilization, extracellular matrix binding, and acute inflammatory response. Using RT-quantitative PCR, we observed differences in the RNA concentrations of certain genes only between the SPB and STB placentas, but not between the STB and term elective cesarean delivery placentas. Notably, 36 RNA transcripts were observed at placental microarray signals higher than a threshold, which indicated the possibility of their detection in maternal plasma. Among them, the IL1RL1 mRNA was tested in plasma samples taken from 37 women. It was detected in 6 of 10 (60%) plasma samples collected during the presentation of preterm labor (≤32.9 weeks) in women eventually giving SPB, but was detected in only 1 of 27 (4%) samples collected during matched gestational weeks from women with no preterm labor (Fisher exact test, p = 0.00056). Conclusion We have identified 36 SPB-associated RNA transcripts, which are possibly detectable in maternal plasma. We have illustrated that the IL1RL1 mRNA was more frequently detected in predelivery maternal plasma samples collected from women resulting in SPB than the gestational-age matched controls.

[1]  S. Moore,et al.  An investigation into the association among preterm birth, cytokine gene polymorphisms and periodontal disease , 2004, BJOG : an international journal of obstetrics and gynaecology.

[2]  L. Poon,et al.  Clinical Chemistry 47:9 1607–1613 (2001) Molecular Diagnostics and Genetics Effects of Blood-Processing Protocols on Fetal and Total DNA Quantification in Maternal Plasma , 2001 .

[3]  Eric P. Skaar,et al.  Small Molecule Inhibitors of Staphylococcus aureus RnpA Alter Cellular mRNA Turnover, Exhibit Antimicrobial Activity, and Attenuate Pathogenesis , 2011, PLoS pathogens.

[4]  Brad T. Sherman,et al.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.

[5]  M. Aidoo,et al.  Tumor necrosis factor‐α promoter variant 2 (TNF2) is associated with pre‐term delivery, infant mortality, and malaria morbidity in western Kenya: Asembo Bay Cohort Project IX , 2001, Genetic epidemiology.

[6]  R. Romero,et al.  The preterm parturition syndrome , 2006, BJOG : an international journal of obstetrics and gynaecology.

[7]  S. Witkin,et al.  Interleukin-4 and -10 gene polymorphisms and spontaneous preterm birth in multifetal gestations. , 2004, American journal of obstetrics and gynecology.

[8]  Chunming Ding,et al.  Detection of the placental epigenetic signature of the maspin gene in maternal plasma. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[9]  N. Chegini,et al.  Expression Profile of MicroRNAs and mRNAs in Human Placentas From Pregnancies Complicated by Preeclampsia and Preterm Labor , 2011, Reproductive Sciences.

[10]  P. Nathanielsz,et al.  Printed in U.S.A. Copyright © 1999 by The Endocrine Society Suppression Subtractive Hybridization Identified a Marked Increase in Thrombospondin-1 Associated with Parturition in Pregnant Sheep Myometrium* , 2022 .

[11]  Rafael A Irizarry,et al.  Exploration, normalization, and summaries of high density oligonucleotide array probe level data. , 2003, Biostatistics.

[12]  E. Norwitz,et al.  Intra-Amniotic Infection Upregulates Decidual Cell Vascular Endothelial Growth Factor (VEGF) and Neuropilin-1 and -2 Expression: Implications for Infection-Related Preterm Birth , 2009, Reproductive Sciences.

[13]  Louis J. Muglia,et al.  Genetic contributions to preterm birth: Implications from epidemiological and genetic association studies , 2008, Annals of medicine.

[14]  R. Romero,et al.  Angiogenesis gene expression in mouse uterus during the common pathway of parturition. , 2008, American journal of obstetrics and gynecology.

[15]  Ming-Tseh Lin,et al.  Adverse outcomes after preterm labor are associated with tumor necrosis factor-alpha polymorphism -863, but not -308, in mother-infant pairs. , 2004, American journal of obstetrics and gynecology.

[16]  Roberto Romero,et al.  Epidemiology and causes of preterm birth , 2008, The Lancet.

[17]  M. Krohn,et al.  Tumor Necrosis Factor–α Promoter Gene Polymorphism ‐308 and Chorioamnionitis , 2003 .

[18]  M. Dombrowski,et al.  Proteomic identification of serum peptides predicting subsequent spontaneous preterm birth. , 2011, American journal of obstetrics and gynecology.

[19]  J. Castle,et al.  Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs , 2005, Nature.

[20]  Chris Mungall,et al.  AmiGO: online access to ontology and annotation data , 2008, Bioinform..

[21]  L Deligdisch,et al.  Fetal fibronectin in cervical and vaginal secretions as a predictor of preterm delivery. , 1991, The New England journal of medicine.

[22]  L. Peltonen,et al.  Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis , 2011, PLoS genetics.

[23]  C. Mullighan,et al.  Interleukins-1, -4, -6, -10, tumor necrosis factor, transforming growth factor-beta, FAS, and mannose-binding protein C gene polymorphisms in Australian women: Risk of preterm birth. , 2004, American journal of obstetrics and gynecology.

[24]  M. Taggart,et al.  Stretch Activates Human Myometrium via ERK, Caldesmon and Focal Adhesion Signaling , 2009, PloS one.

[25]  Charles R Cantor,et al.  Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection , 2007, Nature Medicine.

[26]  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.

[27]  T. Leung,et al.  Detection and characterization of placental microRNAs in maternal plasma. , 2008, Clinical chemistry.

[28]  Samuel Parry,et al.  A polymorphism in the promoter region of TNF and bacterial vaginosis: preliminary evidence of gene-environment interaction in the etiology of spontaneous preterm birth. , 2004, American journal of obstetrics and gynecology.

[29]  L. Shulman Noninvasive diagnosis of intraamniotic infection: proteomic biomarkers in vaginal fluid , 2010 .

[30]  N. Uldbjerg,et al.  Preterm delivery , 2005, Acta obstetricia et gynecologica Scandinavica.

[31]  T. Leung,et al.  Development of extraction protocols to improve the yield for fetal RNA in maternal plasma , 2009, Prenatal diagnosis.

[32]  M. Ashburner,et al.  Gene Ontology: tool for the unification of biology , 2000, Nature Genetics.

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

[34]  W. Göpel,et al.  Polymorphisms of genes involved in innate immunity: association with preterm delivery. , 2004, Molecular human reproduction.

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

[36]  V. Beneš,et al.  The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. , 2009, Clinical chemistry.

[37]  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.

[38]  J. Lapidus,et al.  Insights into the multifactorial nature of preterm birth: proteomic profiling of the maternal serum glycoproteome and maternal serum peptidome among women in preterm labor. , 2010, American journal of obstetrics and gynecology.

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

[40]  E. Thom,et al.  The length of the cervix and the risk of spontaneous premature delivery. National Institute of Child Health and Human Development Maternal Fetal Medicine Unit Network. , 1996, The New England journal of medicine.

[41]  I. Blair,et al.  Identification and quantification of preterm birth biomarkers in human cervicovaginal fluid by liquid chromatography/tandem mass spectrometry. , 2009, Journal of proteome research.

[42]  Yonghua Hu,et al.  Tumor necrosis factor-alpha gene G308A polymorphism is associated with the risk of preterm delivery. , 2003, Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences.

[43]  J. Lapidus,et al.  Diagnosis of intra-amniotic infection by proteomic profiling and identification of novel biomarkers. , 2004, JAMA.

[44]  S. Brennecke,et al.  Molecular Markers of Preterm Labor in the Choriodecidua , 2010, Reproductive Sciences.