Department of Cell Biology & Biochemistry, Texas Tech University Health Sciences Center, Lubbock, Texas, United States of America.
Department of Pathology, Texas Tech University Health Sciences Center, Lubbock, Texas, United States of America.
PLoS One. 2018 Jul 5;13(7):e0200211. doi: 10.1371/journal.pone.0200211. eCollection 2018.
Hltf is regulated by intron retention, and global Hltf-deletion causes perinatal lethality from hypoglycemia. In heart, full-length Hltf is a transcriptional regulator of Hif-1α that controls transport systems. Thus, we tested the hypothesis that Hltf deletion from placenta caused or exacerbated neonatal hypoglycemia via Hif-1α regulation of nutrient transporters. RNA-seq data analyses identified significant changes in transcript expression and alternative splicing (AS) in E18.5 placentome. iPathwayGuide was used for gene ontology (GO) analysis of biological processes, molecular functions and cellular components. Elim pruning algorithm identified hierarchical relationships. The methylome was interrogated by Methyl-MiniSeq Epiquest analysis. GO analysis identified gene enrichment within biological processes. Protein expression was visualized with immunohistochemistry. Although two Hltf mRNA isoforms are quantifiable in most murine tissues, only the truncated Hltf isoform is expressed in placenta. The responsible intron retention event occurs in the absence of DNA methylation. iPathwayGuide analysis identified 157 target genes of 11,538 total genes with measured expression. These were obtained using a threshold of 0.05 for statistical significance (p-value) and a long fold change of expression with absolute value of at least 0.6. Hltf deletion altered transcription of trophoblast lineage-specific genes, and increased transcription of the Cxcr7 (p = 0.004) gene whose protein product is a co-receptor for human and simian immunodeficiency viruses. Concomitant increased Cxcr7 protein was identified with immunolabeling. Hltf deletion had no effect on transcription or site-specific methylation patterns of Hif-1α, the major glucose transporters, or System A amino acid transporters. There was no measureable evidence of uteroplacental dysfunction or fetal compromise. iPathGuide analysis revealed Hltf suppresses cytolysis (10/21 genes; p-value 1.900e-12; p-value correction: Elim pruning; GO:019835) including the perforin-granzyme pathway in uterine natural killer cells. Our findings 1) prove the truncated Hltf protein isoform is a transcription factor, 2) establish a functional link between AS of Hltf and immunosuppression at the feto-maternal interface, 3) correlate intron retention with the absence of DNA methylation, and 4) underscore the importance of differential splicing analysis to identify Hltf's functional diversity.
Hltf 通过内含子保留进行调控,全局 Hltf 缺失会导致低血糖引起的围产期致死。在心脏中,全长 Hltf 是 Hif-1α 的转录调节剂,可控制运输系统。因此,我们假设通过 Hif-1α 调节营养转运体,胎盘内 Hltf 的缺失会导致或加重新生儿低血糖症。RNA-seq 数据分析鉴定出 E18.5 胎盘组织中存在大量转录物表达和选择性剪接(AS)的显著变化。iPathwayGuide 用于对生物学过程、分子功能和细胞成分的基因本体论(GO)分析。消除修剪算法确定了层次关系。通过 Methyl-MiniSeq Epiquest 分析来检测甲基组。GO 分析鉴定出生物过程中的基因富集。通过免疫组织化学来可视化蛋白质表达。尽管在大多数鼠组织中都可检测到两种 Hltf mRNA 异构体,但只有截断的 Hltf 异构体在胎盘内表达。这种负责的内含子保留事件发生在没有 DNA 甲基化的情况下。iPathwayGuide 分析鉴定出 11538 个总基因中 157 个目标基因的表达情况。这些基因的获取阈值为 0.05(p 值)和表达绝对值至少为 0.6 的长折叠变化。Hltf 缺失改变了滋养层谱系特异性基因的转录,并增加了 Cxcr7(p=0.004)基因的转录,该基因的蛋白质产物是人类和猿猴免疫缺陷病毒的共受体。免疫标记鉴定到伴随的 Cxcr7 蛋白增加。Hltf 缺失对 Hif-1α、主要葡萄糖转运体或系统 A 氨基酸转运体的转录或特异性甲基化模式没有影响。没有可测量的证据表明胎盘功能障碍或胎儿受损。iPathGuide 分析表明,Hltf 抑制细胞溶解(10/21 个基因;p 值 1.900e-12;p 值校正:消除修剪;GO:019835),包括子宫自然杀伤细胞中的穿孔素-颗粒酶途径。我们的研究结果 1)证明了截断的 Hltf 蛋白异构体是一种转录因子,2)在胎儿-母体界面建立了 Hltf 的 AS 与免疫抑制之间的功能联系,3)将内含子保留与缺乏 DNA 甲基化联系起来,4)强调了差异剪接分析在确定 Hltf 功能多样性方面的重要性。