GTP-Binding Protein 1-Like (GTPBP1l) Regulates Vascular Patterning during Zebrafish Development

Abstract

Genetic regulation of vascular patterning is not fully understood. Here, we report a novel gene, gtpbp1l (GTP-binding protein 1-like), that regulates vascular development in zebrafish. Amino acid sequence comparison and a phylogenetic study showed that gtpbp1l is conserved in vertebrates. Gtpbp1l mRNA is expressed in the vasculature during embryogenesis. Knockdown of gtpbp1l by morpholino impairs the patterning of the intersegmental vessel (ISV) and caudal vein plexus (CVP), indicating the role of gtpbp1l in vasculature. Further apoptosis assays and transgenic fish tests suggested that vascular defects in gtpbp1l morphants are not due to cell death but are likely caused by the impairment of migration and proliferation. Moreover, the altered expression of vessel markers is consistent with the vascular defects in gtpbp1l morphants. Finally, we revealed that gtpbp1l is regulated by VEGF/notch and BMP signaling. Collectively, these findings showed that gtpbp1l plays a critical role in vascular patterning during zebrafish development.

1. Introduction

The right patterning and function of the vascular network in vertebrates are essential for delivering nutrients or oxygen and removing waste. During embryogenesis, failure to form a properly functioning vasculature causes embryonic lethality [1]. The de novo formation of new vessels, termed vasculogenesis and angiogenesis, is a process in which additional vessels sprout and grow from preexisting vascular structures [2].

Zebrafish are gaining popularity among other vertebrate models in various fields, addressing mechanisms relative to blood vessel development including angioblast specification [3], artery-veinous specification [4], and patterning and morphogenesis [5,6,7]. Angioblast progenitors specify arteries and veins primarily via VEGF–Notch signaling interplay. Further, angioblasts sprout, proliferate, and migrate from the preexisting main vessels to form a secondary vessel network, such as intersegmental vessels (ISVs) in the zebrafish trunk. The timing and directions are mediated by several molecules during the growth of ISVs [8,9]. However, these mediators have not been completely characterized with respect to angiogenesis during the development of embryos. One of the endothelial progenitor cells called the tip cell receives and follows guidance cues, while the other stalk cells trail up and form a lumen [10]. Previously, several pathways were linked to tip–stalk cell specification, which includes Notch and VEGFC/VEGR3 [10,11]. The regulators and molecular signals that govern the specification of tip and stalk cells are still vague. In addition to the angiogenesis of ISV, endothelial progenitor cells also sprouted ventrally from the posterior cardinal vein to form a honeycomb-like vessels network called the caudal vein plexus (CVP) via BMP signal pathways [12,13]. However, their regulators and mechanism have largely remained uncertain.

GTPases are key proteins in many critical biological processes. The small GTPase Rap1 has been shown to promote VEGFR2 activation and angiogenesis [14]. Members of the Ras GTPase family have been shown to function in vascular patterning via semaphorin-Plexin signaling [15]. The G-protein-coupled receptor GPCR126 is involved in pathological and developmental angiogenesis by regulating VEGFR2 signals [16]. In addition to typical small GTPases and GPCRs, the GTP-binding protein superfamily includes the putative GTPase encoded by the Gtpbp1l (GTP binding protein 1-like) gene. The encoded amino acid sequence of this protein showed the highest homology with human GTPBP1. GTPBP1 possesses eEF1A-like elongation activity, delivering aa-tRNA to the A site of the ribosome in a GTP-dependent manner. Thus, GTPBP1 is classified as a translational GTPase (trGTPase) superfamily [17]. Furthermore, GTPBP1 has been shown to interact with exosomes and can stimulate the exosomal degradation of mRNAs engaged within elongation complexes [18]. A recent study showed that tRNA deficiency leads to ribosomal arresting and neurodegeneration and GTPBP1 resolves stalled ribosomes to regulate neuronal homeostasis during defective elongation [19]. However, there have been no reports on the function of the GTPBP superfamily in vessels.

Here, we report a novel gtpbp1l gene that controls vascular development in zebrafish. We showed that Gtpbp1l mRNA is expressed in developing vessels, and a loss of gtpbp1l impairs the patterning of ISV and CVP, indicating the role of gtpbp1l in vasculature. We further showed vascular defects are likely caused by the impairment of migration and proliferation. Furthermore, the reduced expression of vessel genes is consistent with the vascular defects in gtpbp1l morphants. We also revealed that gtpbp1l is regulated by VEGF/notch and BMP signals. Together, these findings showed that gtpbp1l plays a critical role in vascular development.

2. Materials and Methods

2.1. Zebrafish and Chemical Treatments

Zebrafish were raised at 28.5 °C as recommended [20] and managed according to regulations referred by the Institutional Animal Care Committee NSYSU (IACUC no. 10752). Wild-type AB or TL fish and transgenic lines Tg(kdrl:eGFP)^la116, Tg(kdrl:mCherry)^ci5, and Tg(fli1a:negfp)^y7 [21] were obtained from the Zebrafish Core Facility in Taiwan. Furthermore, 0.003% 1-phenyl-2-thiourea (PTU, Sigma, St. Louis, MO, USA) was added to the fish medium to prevent pigment formation of embryos at 6 h post-fertilization (hpf). DAPT, SU5416, Dorsomorphin (DM), and DMH1 (Sigma) were used to inhibit the respective pathways, and DMSO was used as the control.

2.2. Morpholino and mRNA Injection

Microinjections were performed with borosilicate filament glass microcapillaries that were pulled with a P-97 micropipette puller (Sutter Instrument, Novato, CA, USA). Morpholinos (MOs) were obtained from the Gene-Tools company (Philomath, OR, USA). Morpholinos were designed to block the translation of gtpbp1l by targeting the first codon (gtpbp1l^atg MO) or disrupt the splicing of gtpbp1l (gtpbp1l ^e4i4MO) by targeting the exon 4-intron 4 boundary; the MO sequences were as follows:

gtpbp1l ^atgMO: 5′-GCTGCTTCAGCATCTGTCTGGAAAA-3′;

gtpbp1l ^e4i4MO: 5′-GCACACCTACTGCCTCTCACCATTA-3′.

The quantities of morpholinos injected were 3.4 ng and 8 ng, respectively. For rescue experiments, we generated a gtpbp1l mRNA expression construct using Tol2kit vectors with the multisite Gateway cloning system (Invitrogen, Philadelphia, PA, USA). The gtpbp1l-coding region flanking the attb1/b2 sequences was amplified from cDNA by using the primers listed in Table S1 to generate pDONR-gtpbp1l. Capped and polyadenylated gtpbp1l mRNA was synthesized in vitro using the mMESSAGE mMACHINE transcription kit with SP6 RNA polymerase (Ambion, Austin, TX, USA). All injections were performed on one-cell zebrafish embryos by using a FemtoJet microinjector (Eppendorf, Hamburg, Germany).

2.3. RNA Extraction and RT–qPCR Assays

Total RNA was isolated using the RNeasy kit (Qiagen, Valencia, CA, USA) and mRNA was reverse transcribed to cDNA using the oligo-dT primer (Roche Applied Science, Branford, CT, USA) based on the manufacturer’s protocols. Quantitative PCR was performed using reagent SYBR Green Mix (Roche), and qPCR primers used in this study are listed in Table S1. The relative expression of respective genes was analyzed and calculated by the ΔΔCt method by considering β-actin as an internal control. All biological experiments were performed in triplicate.

2.4. Whole-Mount In-Situ Hybridization and Cryosectioning

The in situ probe generation for ephrinb2, mrc1, flt4, and stabilin was described previously [22]. The gtpbp1l 0.5 kb fragment was obtained by PCR amplification using the primers listed below and the PCR product was cloned into the pGMT Easy vector (Promega, Madison, WI, USA). The plasmids were linearized and subjected to in vitro transcription using T7 or SP6 RNA Polymerase (Roche) with a DIG-labeled RNA labeling kit (Roche) to synthesize antisense and sense probes, respectively, for in situ hybridization.

gtpbp1l-f: 5′-GCAGTCCAGCAAGAAACCTCC-3′

gtpbp1l-r: 5′-CGGTTTTATCCACCGTGATT-3′

Briefly, regarding the hybridization procedure, the embryos were fixed using 4% paraformaldehyde (PFA) and stored at −20 °C in methanol for dehydration until further use. After cycles of rehydration, embryos were permeabilized with 10 µg/mL of Proteinase K (Roche). Then the embryos were incubated with respective probes at 65°C overnight and blocked with 1% BSA for 2 h. Embryos were then incubated with AP-conjugated anti-DIG antibody overnight at 4 °C. After several wash steps to remove extra antibodies, an NBT and BCIP substrate (Roche) was used for color development. Embryos were photographed via embedding in 3% methylcellulose. For cryo-sectioning, embryos were fixed with the TekOCT tissue freezing medium, sectioned at approximately 10 µm thickness using a Leica CM3050S cryostat (Leica Biosystems, Deer Park, TX, USA), and photographed.

2.5. Image Processing and Analysis

Methyl cellulose (Sigma) or low-melting agarose (Invitrogen) are used for embryo embedding. White-light or fluorescent images were photographed with a high-resolution camera Axiocam (Carl Zeiss, Jena, Germany) on the Lumar V12 stereomicroscope and photos were processed by AxioVision software. For the confocal photos, embryos were embedded in low-melting agarose with 5% tricaine to immobilize them, and images were collected on Zeiss LSM700 confocal microscopes and processed in ZEN software (Carl Zeiss) or ImageJ software (NIH, Bethesda, MD, USA).

2.6. TUNEL Assay

The protocol of the TUNEL assay for apoptotic cell detection is based on a previous publication [22,23]. Briefly, embryos were fixed in PFA and dehydrated in methanol until use. After rehydration and permeabilization, apoptotic cells were detected by a TUNEL assay kit (Roche) according to the manufacturer’s instructions. The fixed embryos were treated with 3% H₂O₂, washed, and labeled with the TUNEL enzyme. After being washed to remove extra non-incorporated nucleotides and blocked with 5% sheep serum, embryos were then incubated with the peroxidase (POD)-conjugated anti-fluorescein antibody (Roche) overnight at 4°C. Color development was visualized using a DAB kit (Roche).

2.7. Acridine Orange Staining

Embryos were dechorionated and cultured in a fish medium containing 2 µg/mL acridine orange (AO, Sigma) for 40 min. To remove extra acridine orange, embryos were washed six times with a fresh fish medium. The embryos were then embedded in 3% methylcellulose and photographed.

2.8. Statistical Analysis

Data are presented as the mean ± standard deviation (SD). A one-way analysis of variance (ANOVA) was used to compare multiple groups. The difference between the two groups was evaluated using Student’s t-test. p values < 0.05 were considered statistically significant.

3. Results

3.1. Gtpbp1l Is Expressed in Developing Vessels

We are interested in identifying molecules that are required for vascular patterning. The gtpbp1l (GTP binding protein 1-like) gene was identified as a potential target in our previous transcriptome screening for genes regulated by the transcription factor islet2/nr2f1b [24]. Gtpbp1l encodes a putative GTPase and belongs to the GTP-binding protein superfamily. Its deduced amino acid sequence exhibited the highest overall homology with human GTPBP1 (Figure S1). To determine gtpbp1l’s role in zebrafish vasculature, we performed whole-mount in situ hybridization. At the 18 somite stage (S), it is expressed in the eyes, brain, head, and lateral plate mesoderm (lpm) (Figure 1A). Expression at the lpm corresponds to its localization in developing vessels. At 24 hpf, it is expressed in the eyes, brain, vessels (v), and caudal vein plexus (CVP) in the trunk (Figure 1B,B’). At 30 and 48 hpf, it continued to be expressed in the trunk, especially in the vessels, intersegmental vessels (ISVs), dorsal longitudinal anastomotic vessels (DLAV), and CVP (Figure 1D–F). Transverse sections of the 48 hpf embryo further confirm its expression in primary vessels such as the dorsal aorta (DA), posterior cardinal vein (PCV), and CVP (Figure 1E’,F’). These data show the expression of gtpbp1l in developing vessels and suggest the function of gtpbp1l in vascular development.

3.2. Knockdown of gtpbp1l Causes Vascular Defects during Zebrafish Embryogenesis

We took advantage of using transgenic Tg (kdrl:eGFP) zebrafish expressing GFP in endothelial cells to test the potential function of gtpbp1l in vascular formation during embryogenesis. We knocked down gtpbp1l gene expression by microinjection of 3.4 ng of morpholino (gtpbp1l^atg MO) to block the ATG translational site. The loss of gtpbp1l resulted in two obvious vascular phenotypes, ISV growth defects, and CVP mispatterning (Figure 2A–F,K,L). At 30 hpf, approximately 48% of gtpbp1l^atg morphants had complete ISVs (n = 32 embryos) compared to 95% of uninjected control embryos (n = 35 embryos). Meanwhile, a secondary phenotype we observed was CVP formation during embryogenesis. At 30 and 48 hpf in the wild-type fish, endothelial cells in the CVP region showed angiogenic sprouting, migration, fusion, and formed honeycomb-like structures or loops (Figure 2C–F). There was less or no honeycomb structure in the CVP in injected embryos compared to the uninjected controls at 30 hpf (Figure 2C,D). At 48 hpf, the swallowed plexus with less or no loops at CVP can be observed and quantified in gtpbp1l morphants (n = 33) (Figure 2E,F).

Consistent with the vasculature defects in gtpbp1l morphants, we found that a loss of gtpbp1l resulted in circulation defects and pericardial edema at 48 hpf and 72 hpf. At 48 hpf, we examined the circulation in wild-type and morphants and noted limited blood flow in the trunk of gtpbp1l 1 morphants. Among gtpbp1l morphants, ~40% of Tg (fli1a:eGFP^y1; gata1:dsRed^sd2) embryos exhibited circulation in the axial vessels, and only ~10% exhibited ISV circulation (Figure 2G,H, n = 25 in control and n = 23 in gtpbp1l ^ATG MO) (Figure 2M). At 72 hpf, we found that a loss of gtpbp1l caused increased pericardial edema in ~90% of embryos (Figure 2I–N, n = 30 in control and n = 26 in gtpbp1l^atg MO) (Figure 2N). Edema and circulation defects are common side effects of blood vessel impairment. These data correlated with the vasculature defects in the gtpbp1l knockdown embryos.

3.3. Specificity of gtpbp1l Knockdown by Morpholino Injection

In Figure 2, we found that knockdown of gtpbp1l by inhibiting the translation ATG start site (gtpbp1l^atg MO) impairs vascular development. To demonstrate the phenotypic specificity of gtpbp1l morpholino knockdown, we designed a second morpholino (gtpbp1l^e4i4 MO) that interferes with gtpbp1l pre-RNA splicing at the exon 4-intron 4 boundary and examined the effects in vasculature. Our data showed that the phenotype of vascular defects in gtpbp1l^e4i4MO (Figure S2) fish wasa very similar to those in the gtpbp1l^atg morphants. We observed vascular defects in CVP formation and ISV growth, with a 34% decrease at 30 hpf (Figure S2A–F,I,J). A vascular defect in CVP loops formation was also observed at 48 hpf (Figure S2E,F). We also found edema in gtpbp1l^e4i4 MO at 72 hpf (Figure S2G,H,K). We further examined the efficiency of gtpbp1l^e4i4 morpholino knockdown by RT–PCR analysis. As the data showed, the injection of 8 ng of gtpbp1l^e4i4 morpholino decreased the level and mis-spliced fragments of gtpbp1l (Figure S2L,M), indicating the gtpbp1l^e4i4 morpholino inhibition of the gtpbp1l gene is efficient. These results also confirmed that the vascular defects caused by gtpbp1l knockdown are specific.

We further performed rescue experiments by overexpressing gtpbp1l in wild-type and gtpbp1l^e4i4 morphant embryos to examine the specificity that vascular defects caused by morpholino knockdown. The overexpression of gtpbp1l in wild-type embryos had no obvious effect on vascular ISV and CVP development compared to the wt control (Figure 3A,E,C,G). However, we found that the overexpression of gtpbp1l mRNA in gtpbp1l MO can restore ISV growth to form DLAV by 36% compared to the knockdown of gtpbp1l (gtpbp1l MO) at 28 hpf (Figure 3D,B,I). In addition, at 52 hpf, overexpression of gtpbp1l mRNA rescued the CVP defect in an additional 47% of embryos compared to gtpbp1l MO as the baseline (Figure 3E–H,J). Our data also suggested that general development in other tissues and organs was unaffected since the knockdown of gtpbp1l at 24–25 hpf did not alter the expression of cmlc2 (heart marker), hbee1 (blood marker), myoD (somite marker), shh (floor plate marker), or sox3 (neural marker) (Figure S3A–J). Together, these data suggest that the loss of gtpbp1l causes vascular defects that are gene-knockdown-specific and phenotype-specific.

3.4. Loss of gtpbp1l Impairs the Growth of ISV Cells

Loss of gtpbp1l results in vascular growth defects, suggesting the growth or survival interruption of endothelial cells. To evaluate whether endothelial cells suffer the problems of proliferation, migration, or cell death, we first examined apoptotic cells by using a TUNEL assay and Acridine orange staining. We showed that gtpbp1l morphants have slightly increased apoptosis (apoptotic spots) in the dorsal and epidermal region compared to uninjected wt control embryos at 30hpf. However, morpholino-induced cell death is not present in the vessel region of the trunk by checking vessel mCherry signals (Figure 4A–D), indicating that the vascular defect of gtpbp1l morphants is not due to the death of endothelial cells. To examine whether the loss of gtpbp1l affects cell proliferation, we counted the number of endothelial cells per ISV in the Tg(kdrl:mCherry;fli1a:negfp ^y7) embryos. gtpbp1l morphants showed significantly decreased ISV cells compared to the wild-type control (Figure 4E–G, n = 30 in gtpbp1l morphants and n = 30 in wt control). Moreover, fewer ISV cells can migrate to the top of the embryo to form DLAVs, suggesting the interruption of ISV endothelial cell migration in gtpbp1l Mos. These data suggested that gtpbp1l is critical for endothelial cell growth to form ISVs and CVP, likely via regulating cell proliferation, migration, or both.

3.5. Knockdown of gtpbp1l Alters the Expression of Vessel Genes

The observed vascular defects in ISV and CVP suggest gtpbp1l’s role in the vasculature to modulate vascular identity. To determine how it is affecting vascular markers, we checked their expression via in situ hybridization and qPCR. We examined typical vascular markers including flk, flt4, mrc1, stabilin, and ephrinb2 at 24 hpf. We noted the expression of the flk and stabilin (pan-vascular markers), flt4 (venous/ISV marker), and mrc1 (venous marker) was reduced significantly in the gtpbp1l knockdown group compared to wild-type controls (Figure 5). The relative expression of these markers shows a reduction of approximately 30–50% in their expression in the knockdown group. These results indicate gtpbp1l’s role in the regulation of vascular genes to control the development of healthy vessels.

3.6. Interaction between gtpbp1l and Multiple Signals

Our data showed that the loss of gtpbp1l interrupted the growth and patterning of ISVs and CVP. Notch signaling is crucial for the specification of venous cells and ISV tip cells and important for the migration and proliferation of endothelial progenitor cells via the interaction with VEGFR2 signaling during angiogenesis in the zebrafish trunk. Therefore, we tested the regulatory relationships between gtpbp1l and Notch or VEGFR2. We inhibited Notch and VEGFR2 signaling through exogenous DAPT and SU5416 treatment, respectively (Figure 6A–D). We found that the expression of gtpbp1l was downregulated when Notch or VEGFR2 signals were inactivated. These data suggest that gtpbp1l controls vascular patterning and is likely regulated by the Notch and VEGF pathways.

In addition, BMP signaling was reported to regulate angiogenic sprouting from the axial vein to pattern the CVP, which provides a different regulating mechanism of angiogenesis from ISV growth [12,13]. We therefore tested whether gtpbp1l interacts with BMP signaling to function in CVP formation by using BMP signaling inhibitors DMH1 and DM. Compared with DMSO treatment as a control, DM or DMH1 treatment reduced the expression level of gtpbp1l in the embryos (Figure 6E–H). These data suggest that gtpbp1l is downregulated by BMP signaling. Collectively, these results suggest that gtpbp1l controls ISV and CVP through VEGF/Notch and BMP signaling.

4. Discussion

GTPase proteins have been shown to be involved in many important biological processes. They encompass a large group of enzymes that bind GTP and undergo a conformational change as GTP is hydrolyzed to GDP. The main groups of GTPases are heterotrimeric G-proteins (G-coupled receptors, GPCRs) and small GTPases (including several superfamilies, e.g., Ras, Rho/Rac/Cdc42, Rap, Ran, and Arf) [25,26,27]. The coordinated activation of Rho GTPases by signals is required for angiogenic processes, including cell guidance, migration, proliferation, and morphogenesis [28]. The regulation of Rho GTPase activation is mediated by interactions with guanine nucleotide exchange factors (GEFs) or GTPase-activating proteins (GAPs). Many GEFs have been shown to regulate angiogenesis and vascular function by fine-tuning the actions of Rho GTPase [26]. Vascular malformations are linked to mutations in RAS p21 protein activator 1 (Rasa1 or p120RasGAP). Kawassaki et al. showed that Rasa1/Ras interacts with the Ephb4 signaling pathway to suppress endothelial mTORC1 activity and Rasa1 mutation leads to capillary malformation arteriovenous malformations (CM-AVMs) [29]. In addition, recent transcriptome analysis reveals molecular signatures in cerebral cavernous malformation (CCM) endothelial cells, which provides the fundamental role of growth factors and RAS in the field of pathologies related to angiogenesis [30].

Many translational GTPases (trGTPases) are essential for life due to their pivotal roles in the translation cycle on the ribosome. The classical trGTPases (IF2, EF-Tu, EF-G) are highly conserved and well-studied in the function of the translation process. GTP-binding proteins (GTPBPs) comprise a divergent group of translational GTPases with uncertain functions but are closely related to EF1A and RF3 [31]. Although GTPBPs have widespread expression, physiological functions remain limited. Initial studies focused on their tissue specificity, suggesting the role of GTPBP1 and GTPBP2 in innate immunity [32,33]. Recent studies revealed the different biochemical roles of GTPBP1 and GTPBP2 [17,18]. GTPBP1 likely directs the exosome to mRNA targets. GTPBP2 can interact with aa-tRNA but lacks elongation activity and does not promote exosome degradation, suggesting that GTPBP1 and GTPBP2 have different roles. Terrey et al. found that GTPBP1 resolves paused ribosomes to maintain neuronal homeostasis linked to mTOR signals [19]. A study on GTPBP2 showed that ribosome stalling induced by the mutation of a CNS-specific tRNA causes neurological defects [34]. The essential role of Gtpbp2 in neural homeostasis was further revealed by the fact that mutations in Gtpbp2 in humans cause neurodegeneration and intellectual disabilities [34,35]. In addition, Gtpbp2 has been shown to interact with Smad1/BMP signaling and is essential for mesodermal development in Xenopus embryos [36]. Knockout of Gtpbp3 in zebrafish caused hypertrophic cardiomyopathy and showed abnormal mitochondrial tRNA metabolism [37]. In this study, we reported a novel function of the GTPBP superfamily in vascular development, identified in this first investigation of the role of GTPBP in vasculature. We also revealed that gtpbp1l regulates vascular development mediated by VEGF/Notch and BMP signals.

Based on the known biochemical function of GTPBPs, we propose two potential mechanisms by which gtpbp1l regulates vascular development. First, Gtpbp1l is important for vessel growth mediated by proangiogenic protein synthesis, i.e., Gtpbp1l possesses eEF1A-like elongation activity, delivering cognate aminoacyl-transfer RNA (aa-tRNA) to the ribosomal A site in a GTP-dependent manner, supporting the protein synthesis of angiogenesis or angiogenic signals. Second, Gtpbp1l regulates vessel growth mediated by exosome-dependent mRNA degradation of antiangiogenic factors. Similar to AANAT (aralkylamine N-acetyltransferase), mRNA turnover is controlled by the interaction between GTPBP1 and exosomes [18]. Thus, GTPBP1l may act as a regulator and adaptor of the exosome-mediated mRNA turnover pathway. In addition, exosomes (extracellular vesicles) have been shown to carry microRNAs or ligands (VEGF, PDGF, etc.) that are important for angiogenesis; thus, the disruption of exosome trafficking, docking, or release might impair vascular growth [38]. Xu et al. showed that neurons secrete miR-132-containing exosomes to regulate brain vascular integrity and miR132 knockdown impairs vascular integrity in zebrafish [39].

It has been reported that Gtpbp2 interacts directly with Smad1 to regulate BMP signaling and is essential for mesoderm development in a frog model. How gtpbp1l interacts with VEGF or BMP signals will be interesting to address. The translation is highly regulated by two signal pathways: The mTOR signaling and the integrated stress response (ISR) [40]. Whether gtpbp1l regulates vessel growth mediated by mTOR signals is also intriguing. Finally, a mammalian study suggested functional redundancy between Gtpbp1 and Gtpbp2 [33]. Zebrafish Gtpbp1 is expressed in the blood during embryogenesis, suggesting its function in blood development. Whether GTPBP1 has vascular function is not known and will be interesting to address.

5. Conclusions

In this study, we report a novel gene, gtpbp1l (GTP-binding protein 1-like), that controls vascular development in zebrafish. We showed that gtpbp1l mRNA is expressed in the vasculature, and the knockdown of gtpbp1l impairs the growth of ISVs and the CVP. We further showed vascular defects are likely caused by the impairment of migration and proliferation. We also revealed that gtpbp1l is regulated by VEGF and BMP signals. These findings showed that gtpbp1l plays a critical role in vascular development. To our knowledge, the novel function of gtpbp1l in the genetic network during vascular development has never been explored.