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人类胎盘的高通量mRNA测序显示整个妊娠期存在性别差异。

High-throughput mRNA sequencing of human placenta shows sex differences across gestation.

作者信息

Flowers Amy E, Gonzalez Tania L, Wang Yizhou, Santiskulvong Chintda, Clark Ekaterina L, Novoa Allynson, Jefferies Caroline A, Lawrenson Kate, Chan Jessica L, Joshi Nikhil V, Zhu Yazhen, Tseng Hsian-Rong, Wang Erica T, Ishimori Mariko, Karumanchi S Ananth, Williams John, Pisarska Margareta D

机构信息

Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.

Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.

出版信息

Placenta. 2024 May;150:8-21. doi: 10.1016/j.placenta.2024.03.005. Epub 2024 Mar 21.

Abstract

INTRODUCTION

Fetal sex affects fetal and maternal health outcomes in pregnancy, but this connection remains poorly understood. As the placenta is the route of fetomaternal communication and derives from the fetal genome, placental gene expression sex differences may explain these outcomes.

OBJECTIVES

We utilized next generation sequencing to study the normal human placenta in both sexes in first and third trimester to generate a normative transcriptome based on sex and gestation.

STUDY DESIGN

We analyzed 124 first trimester (T1, 59 female and 65 male) and 43 third trimester (T3, 18 female and 25 male) samples for sex differences within each trimester and sex-specific gestational differences.

RESULTS

Placenta shows more significant sexual dimorphism in T1, with 94 T1 and 26 T3 differentially expressed genes (DEGs). The sex chromosomes contributed 60.6% of DEGs in T1 and 80.8% of DEGs in T3, excluding X/Y pseudoautosomal regions. There were 6 DEGs from the pseudoautosomal regions, only significant in T1 and all upregulated in males. The distribution of DEGs on the X chromosome suggests genes on Xp (the short arm) may be particularly important in placental sex differences. Dosage compensation analysis of X/Y homolog genes shows expression is primarily contributed by the X chromosome. In sex-specific analyses of first versus third trimester, there were 2815 DEGs common to both sexes upregulated in T1, and 3263 common DEGs upregulated in T3. There were 7 female-exclusive DEGs upregulated in T1, 15 female-exclusive DEGs upregulated in T3, 10 male-exclusive DEGs upregulated in T1, and 20 male-exclusive DEGs upregulated in T3.

DISCUSSION

This is the largest cohort of placentas across gestation from healthy pregnancies defining the normative sex dimorphic gene expression and sex common, sex specific and sex exclusive gene expression across gestation. The first trimester has the most sexually dimorphic transcripts, and the majority were upregulated in females compared to males in both trimesters. The short arm of the X chromosome and the pseudoautosomal region is particularly critical in defining sex differences in the first trimester placenta. As pregnancy is a dynamic state, sex specific DEGs across gestation may contribute to sex dimorphic changes in overall outcomes.

摘要

引言

胎儿性别会影响孕期胎儿和母亲的健康结局,但这种关联仍未得到充分理解。由于胎盘是母婴交流的通道且源自胎儿基因组,胎盘基因表达的性别差异可能解释这些结局。

目的

我们利用下一代测序技术研究了孕早期和孕晚期两性的正常人类胎盘,以生成基于性别和孕周的标准转录组。

研究设计

我们分析了124例孕早期(T1,59例女性和65例男性)和43例孕晚期(T3,18例女性和25例男性)样本,以研究各孕周内的性别差异以及性别特异性的孕周差异。

结果

胎盘在孕早期表现出更显著的性别二态性,孕早期有94个差异表达基因(DEG),孕晚期有26个。性染色体在孕早期贡献了60.6%的差异表达基因,在孕晚期贡献了80.8%的差异表达基因,不包括X/Y假常染色体区域。假常染色体区域有6个差异表达基因,仅在孕早期显著,且在男性中均上调。X染色体上差异表达基因的分布表明,Xp(短臂)上的基因在胎盘性别差异中可能尤为重要。X/Y同源基因的剂量补偿分析表明,表达主要由X染色体贡献。在孕早期与孕晚期的性别特异性分析中,两性共有2815个差异表达基因在孕早期上调,3263个共有差异表达基因在孕晚期上调。孕早期有7个女性特有的差异表达基因上调,孕晚期有15个女性特有的差异表达基因上调,孕早期有10个男性特有的差异表达基因上调,孕晚期有20个男性特有的差异表达基因上调。

讨论

这是来自健康妊娠的整个孕期胎盘的最大队列研究,定义了标准的性别二态性基因表达以及整个孕期性别共有的、性别特异性的和性别特有的基因表达。孕早期具有最多的性别二态性转录本,且在两个孕期中,与男性相比,大多数在女性中上调。X染色体短臂和假常染色体区域在定义孕早期胎盘的性别差异中尤为关键。由于妊娠是一个动态状态,整个孕期性别特异性的差异表达基因可能导致总体结局中的性别二态性变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2098/11262790/d7728ba76371/nihms-1982593-f0001.jpg

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