Long non-coding RNAs during normal erythropoiesis

Changlu Xu,Lihong Shi,*

aState Key Laboratory of Experimental Hematology,National Clinical Research Center for Hematological Disorders,Institute of Hematology and Blood Diseases Hospital,Chinese Academy of Medical Sciences and Peking Union Medical College,Tianjin,China; bCenter for Stem Cell Medicine,Chinese Academy of Medical Sciences & Department of Stem Cells and Regenerative Medicine,Peking Union Medical College,Tianjin,China

Abstract

Keywords:Erythropoiesis,Globin regulation,Heme biosynthesis,Long non-coding RNAs

1.INTRODUCTION

Red blood cells(RBCs)enable to transport oxygen to all tissues over the body,which are generated in the bone marrow via a multistep process named erythropoiesis.During erythropoiesis,the earliest committed erythroid progenitors are burst-forming unit-erythroid(BFU-E)and colony-forming unit-erythroid(CFUE).Then the CFU-E progenitors divide 3 to 5 times over 2 to 3 days as they differentiate and undergo many substantial changes,including a decrease in cell size,chromatin condensation,and hemoglobinization,leading up to enucleation and expulsion of extra organelles,ultimately turning into mature RBCs.1

Recently,with the advances of high throughput RNA-sequencing technology,it has been increasingly appreciated that there are substantial RNAs without protein-coding potential in the cells,termed non-coding RNAs (ncRNAs).Albeit ＞60% of the mammalian genome (～2/3) is capable to be transcribed,protein-coding genes account for ＜2% of these transcribed transcripts in the entire mammal genome.2Such huge amounts of non-coding transcripts could be mainly classified as miRNAs,small interfering RNAs,housekeeping RNAs,and long noncoding RNAs (lncRNAs).3

LncRNAs are transcripts ＞200 nucleotides in length that do not code for proteins.Based on their genomic location and their neighboring protein-coding gene(s),lncRNAs have been further classified into six subgroups: intergenic lncRNAs (lincRNAs),intronic overlapping lncRNAs (ilncRNAs),antisense lncRNAs(alncRNAs),enhancer lncRNAs (elncRNAs),sRNA-host lncRNAs (shlncRNAs),and Pseudogene lncRNAs(plncRNAs).4,5Compared with protein-coding genes,lncRNAs,in general,process the characteristics such as relatively shorter transcript length with 2 to 3 exons,poor conservation across multiple species,lower expression abundance as well as developmentally spatiotemporal specificity.6,7Mechanistically,lncRNAs could regulate its targets through diverse molecular mechanisms.8First,lncRNAs can act as a ribonucleoprotein scaffold to modulate nuclear architecture and regulate gene expression.9Secondly,LncRNAs also can be co-expressed with their neighbor protein-coding genes and regulate their expression.10Thirdly,they can be involved in post-transcriptional RNA modifications,include splicing,editing,etc.11In addition,a small subset of lncRNAs participate in signal transduction and thus control diverse biological processes.12Since very few lncRNAs have been identified during erythroid disorders,in this review,we solely focus on the very recent advances of the functions and mechanisms of lncRNAs during physiological (normal) rather than pathological erythropoiesis.

1.1.LincEPS and LncRNA-Saf in erythroid cell survival

It has been well documented that lncRNAs serve as vital regulatory elements governing diverse cell differentiation processes,including erythropoiesis.Hu et al13first explored lncRNA landscape during mouse erythropoiesis utilizing RNA-seq technology from purified mouse fetal liver erythroid progenitors BFU-Es,CFU-Es,and terminal differentiated Ter119+erythroid cells.They identified ＞400 putative lncRNAs that are expressedduring mouse erythropoiesis.Among them,lincRNA-erythrocyte prosurvival(lincEPS)is highly induced in terminally differentiating erythroblasts.Its inhibition leads to apoptosis and severely impairs differentiation and subsequent enucleation of erythroblasts,while its ectopic expression protects erythroid progenitors from apoptosis,strongly suggesting a potent antiapoptotic activity (Table1).Mechanistically,lincRNA-EPS diffuses throughout the nucleus to repress loci encoding common mediators of apoptotic in red cells,including the caspaseactivating adaptor protein Pycard.In detail,lincRNA-EPS binds the promoters of its target genes,for example Pycard,and promotes nucleosome occupancy near their transcription start site,therefore repressing their expression,which tightly depends on its interacting protein HNRNPL.14However,it still unclear how lincRNA-EPS reaches its targets,which awaits further investigation (Fig.1B).

Table1 Long non-coding RNAs in normal erythropoiesis.

LncRNA Fas-antisense 1(Fas AS1 or Saf)is upregulated at late stages of human erythroid maturation derived from human bone marrow CD34+cells.15Overexpression of this lincRNA in primary erythroid cells protects erythroblasts from Fas-mediated cell death signals.Its upstream regulators are the erythroid lineage specific transcription factors,GATA1 and KLF1,which bind to the promoter of lncRNA-Saf to active its transcription.In conversely,lncRNA-Saf is negatively regulated by NF-κB(Fig.1C).Nonetheless,its downstream targets and the underlying molecular mechanisms in erythroid maturation are still largely unknown.

1.2.AlncRNA-EC7 and ShlncRNA-EC6 during erythroid differentiation

Alvarez-Dominguez et al also profiled lncRNAs in distinct differentiation stages of erythroid cells from mice fetal liver using RNA-seq.5They rigorously filtered out 655 differentially expressed lncRNAs at E14.5 erythroid cells,including 132 previously unannotated lncRNAs.After integrating dynamic expressed lncRNAs with genome-wide surveys of chromatin states and transcription factor occupancy,they revealed that dynamic alteration of lncRNAs expression closely orchestrates with chromatin histone architecture and is targeted by key erythroid transcription factors,including GATA1,TAL1,and KLF1.They further performed the functional validation of 12 dynamically expressed lncRNAs and illustrated that majority of them are involved in erythroid differentiation and enucleation.For example,alncRNA-EC7 acts as an enhancer for SLC4A1,the gene encoding band 3,which is the primary anion exchanger of the erythrocyte,to modulate erythroid maturation.Mechanistically,alncRNA-EC7 executes its enhancer function in trans,serving as a scaffold via binding to the chromatin attachment factor HNRNPU,the nuclear lamina component LMA,other transcription coactivators (e.g.,MYBBP1A) or corepressors (e.g.,HSPA8) (Fig.1D).16Meanwhile,another lncRNA ShlncRNA-EC6,also called DLEU2,its down-regulation significantly disturbs erythroid enucleation in mouse fetal liver,mediated by upregulating Rac1 and its downstream targets PIP5K.Consistently,overexpression of Rac1 results in inducing PIP5K expression and then blocking erythroid enucleation(Fig.1E).17Additionally,transcribed from an enhancer cobound by GATA1 and TAL1,ElncRNA-EC3 likely enhances KIF2A expression during human erythropoiesis,which is a kinesin motor involved in microtubule dynamics required for normal mitotic progression.However,KIP2A functions during erythropoiesis are yet to know.5

1.3.BGLT3 in globin regulation

The human β-globin locus comprises five coding genes,including the embryonic-specific ε (HBE1),fetal-restricted Gγ and Aγ(HBG2 and HBG1),and adult expressed δ and β(HBD and HBB) globin genes,which are sequentially activated during development.The intergenic region between the Aγ-and δ-globin genes contains a pseudogene (HBBP1) and a noncoding gene(BGLT3).BGLT3 is shown to specifically regulate fetal γ-globin expression.18In erythroid cells BGLT3 co-transcribes with gamma-globin and primarily localizes in the nucleus.After combination of the CRISPR/Cas9 mediated whole gene body deletion,transcription start site deletion as well as antisense oligonucleotides (ASOs) mediated knockdown strategies,Ivaldi et al unraveled that BGLT3 locus and transcript have distinct functions.BGLT3gene locus is exclusively involving in transcriptionally activation of fetal gamma globin genes,but not other types of globin genes,via chromatin looping.Whereas BGLT3 transcripts are dispensable for fetal gamma-globin/BGLT3 looping,it instead interacts with the Mediator complex,such as MED12 on chromatin to facilitate fetal γ-globin transcriptional assembly (Fig.1 F).Since elevated fetal hemoglobin levels are capable to alleviate the syndrome of sickle cell disease or β-thalassemia in patients,HBBP1andBGLT3genes seem are two promising therapeutic targets for genome editing for those diseases.

1.4.UCA1 and heme biosynthesis

Figure1.Erythropoies is and possible modes of action of lncRNAs involved in erythropoiesis. (A) Erythropoiesis. The earliest committed erythroid progenitors are bursttforming unit-erythroid(BFU-E)and colony-forming unit-erythroid(CFU-E).During the terminal erythroid differentiation,the CFU-E progenitors divide 3 to 5 times and undergo many substantial changes,including a decrease in cell size,chromatin condensation,and hemoglobinization,leading up to enucleation and expulsion of extra organelles,ultimately turninginto mature redblood cells.Here,Pro-Epresents proerythroblast;baso-Epresents basophilic erythroblast;Ploy-E presentspolychromatic erythroblast;Ortho-E presents orthochromatic erythroblast;Reti presents reticulocyte;RBCs presents red blood cells.(B)LincRNA-EPS,interacting with the RNA-binding protein HNRNPL,binds to the promoter of Pycard to repress its transcription,executing a potent anti-apoptotic activity.(C)LncRNA Saf promotes erythroid cell survival via inhibiting the Fas-mediated cell death signals,which is transcriptionally upregulated by GATA1 and KLF1 while downregulated by NF-κB.(D)AlncRNA-EC7 induces erythroid maturation by enhancing Band 3 expression.Here,alncRNA-EC7 acts as a protein scaffold to carry on its enhancer function by binding to the chromatin attachment factor HNRNPU,the nuclear lamina component LMA and other unknown transcription coactivator(s).(E)ShlncRNA-EC6 promotes erythroid enucleation via regulating Rac1 and its downstream target PIP5K.(F)(left)Cis-regulatory mechanism:BGLT3 gene locus transcriptionally activates fetal γ-globin genes via facilitating chromatin looping between LCR and γ-globin promoters.(right)Tran-regulatory mechanism:albeit BGLT3 transcripts are dispensable for γ-globin/BGLT3 looping,it instead interacts with the Mediator complex,such as MED12 on chromatin to aid γ-globin transcriptional assembly.Here,LCR refers locus control region.(G)lncRNA UCA1 interacts with RNA binding protein PTBP1 to confer ALAS2 mRNA stability,which in turn regulates heme metabolism.

Shi et al has performed RNA sequencing(RNA-seq)at distinct differentiation stages derived from mobilized adult peripheral blood CD34+cells and comprehensively identified 5326 potential long non-coding RNAs.19After profiling the dynamically expressed lncRNAs during erythropoiesis,Liu and coworkers identified that lncRNA UCA1 regulates heme metabolism in human erythroid cells (Table1).20UCA1 expression peaks in proerythroblasts.Consistent with its expression pattern,diminished UCA1 expression blocked the erythroid differentiation at the proerythroblast stage due to the insufficient heme biosynthesis.Mechanistic analysis suggests that UCA1 interacts with RNA binding protein PTBP1 to confer ALAS2 mRNA stability,which is the rate limiting enzyme of heme biosynthesis(Fig.1 G).20This study revealed a new layer of lncRNA dependent,posttranscriptional regulation of ALAS2 mRNA,which might shed more lights on the heme disorders with currently unknown reasons.

1.5.Specie-,tissue-,and cellular-specificity of LncRNA

Despite a subset of lncRNAs are highly conserved,the majority of lncRNAs seem to be species-or lineage-specific.Paralkar and coworkers used RNA-seq to investigate tissue-and specie-specific lncRNAs during mouse and human erythropoiesis.In analyzing transcriptome of erythroblasts,megakaryocytes,and megakaryocyte-erythroid precursors,they identified 1109 potential lncRNAs expressed in mouse,while only 594 in humans.21More importantly,they uncovered ～15%of mouse lncRNAs are detected in humans or vice versa,reflecting dramatic speciesspecificity.In summary,these lncRNAs might help to shape the specie- and lineage-specific phenotypes.

1.6.Conclusions and future perspectives

The rapid development of high throughput transcriptome profiling techniques greatly aids the identification of lncRNAs,which has been exponentially increased for the past decade.Compared with the number of identified lncRNAs in erythroid development and differentiation,the lncRNAs with functional annotation are relatively few.Still,these studies raise interesting questions.

1.It is largely uncertain that the great number of lncRNAs identified during erythropoiesis is exclusively erythroid lineage specific or not.For example,although lncRNA UCA1 abundantly and dynamically expressed in erythroid cells,20it is also highly expressed in spleen and heart.22Since lncRNAs identified in prior studies were predominantly limited in hematopoietic cells/lineages,a broader comparison cross multiple tissues can answer this question soon.

2.It is intriguing to know whether the lncRNAs share the similar expression pattern possibly conduct resembling roles;

3.given that the majority of identified lncRNAs dynamically expressed during erythroid differentiation,it is yet to be known that the same lncRNA play distinct function at different differentiation stage;

4.although an increasing evidence indicates that lncRNAs play crucial roles during malignant hematopoiesis,the functions of lncRNAs in erythroid diseases have less been demonstrated.In future,it is of importance to continually address the function of these potential regulators to answer these questions.Mechanistically,nuclear localized lncRNAs are more frequently targeting genomic regions to modulate gene expression by recruiting chromatin modifying protein,whereas the cytoplasmic lncRNAs are more likely to interact with RNA-binding proteins to stabilize mRNA or participate in the translational regulation.Thus,combined biochemical and cell biology approaches are promising strategies to integrate the underlying molecular mechanisms of lncRNAs during erythroid development and differentiation,which will also provide valuable insights in various erythroid disorders.

ACKNOWLEDGEMENTS

This work was supported by the National Key Research and Development Program of China (2016YFA0102300 and 2017YFA0103102); CAMS Innovation Fund for Medical Sciences (2016-I2M-3-002,2016-I2M-1-018 and 2017-I2M-1-015);National Natural Science Foundation of China(81870089 and 81700105); CAMS Medical Epigenetics Research Center(2018PT31033);Supported by the Fundamental Research Funds for the Central Universities(3332018157);State Key Laboratory of Experimental Hematology Research Grant (157-z18-07).