The expression vectors C1-ORF2, C1-Alux14 and C1-LacZ were constructed as previously described (16). C1-delPolyA vector was obtained by deleting the poly(A) DNA sequence (240 bp) from the C1-ORF2 vector using the MluⅠ and ApaⅠ restriction enzymes.

TU strain zebrafish were purchased from Nanjing Yaoshunyu Biotechnology Co., Ltd. and maintained under a 14/10-h light/dark cycle at 28.0±0.5°C, as previously described (17,18). Experimental procedures were approved by the Institutional Animal Care and Use Committee of Hebei Medical University (approval no. IACUC-Hebmu-2021009). Adult fish were fed twice a day. A total of 10 pairs of adult male and female (>16 weeks) zebrafish (weight, 0.36-0.44 g) were maintained at 28°C and the embryos were obtained from breeding pairs at 8-9 a.m. Fertilized embryos collected within 45 min (1-cell stage embryos) were considered 0 hpf zebrafish embryos (ZEs). Spawns for which the survival rate of the normal embryos up to 24 h was >90% were considered good-quality embryos, whereas survival rate of the normal embryos up to 24 h was <30% was considered to contain poor-quality embryos.

The plasmids were diluted into a buffer of 0.1 mol/l NaCl and 10 mmol/l Tris-HCl (pH 7.2); final concentration of plasmids was 0.1 μg/μl. A total of 1.7 nl plasmid solution was microinjected into ZE animal pole or yolk sac and the embryos were then cultured in a Petri dish to 6, 12, 24, 48 or 72 h at 28°C.

The expression of the EGFP reporter protein in ZEs was observed under a fluorescence microscope (Leica Microsystems GmbH) in 40X at an excitation wavelength of 490 nm. ImageJ software 1.53 (National Institutes of Health) was used to analyze the fluorescence intensity.

The 0 hpf ZEs were collected and 10X embryo buffer was added to the 0 hpf ZEs at a concentration of 1X (0.1 mol/l NaCl, 0.5 mmol/l PMSF, 2 mmol/l dithiothreitol, 0.5 mmol/l EDTA and 10 mmol/l Tris-HCl, pH 7.4). The embryos were crushed using an ultrasonic cell processor (VIBRA-Cell™ Sonics VCX105; Sonics & Materials, Inc.). The homogenized embryos were centrifuged at 13,400 g for 5 min at 4°C and supernatant (ZEL) was collected. The optimal density (OD) was measured by ultraviolet spectrophotometer (UV-2800A; UNICO Instrument Co., Ltd. Shanghai) at 280 nm and the ZEL was subsequently diluted using 1X embryo buffer (0.475, 0.95, 1.90, 3.80 and 7.60 μg/μl).

LV was purified from ZEL as previously described (19). Purified LV was analyzed using Easy-nLC1200 high-performance liquid chromatography (HPLC; Shanghai Luming Biotechnology Co., Ltd.). The purified LV was labeled using fluorescein isothiocyanate (FITC), as described by Li et al (20). Aliquots of 1.7 nl FITC-LV (20 μg/μl) were injected into the animal pole or yolk sac of 0 hpf or 3 hpf ZEs under the stereomicroscope and fluorescence was observed at 72 h after injection. Male zebrafish plasma (MZP) was isolated as described by Medina-Gali et al (21). Globin was extracted from MZP using a Micro Protein PAGE Recovery kit [Real-Times (Beijing) Biotechnology Co., Ltd.] and identified by SDS-PAGE (15% gel), as previously described (22).

A total of two chromatin reconstitution methods were used: Incubation reconstitution, as described by Stein et al (23), and the salt-dialysis reconstitution method described by Lusser and Kadonaga (24).

In incubation reconstitution process (7,25), plasmids were diluted into plasmid solution to a final concentration of 0.1 μg/μl. Each plasmid was incubated with histone octamer (0.000, 0.005, 0.010, 0.020, 0.040, 0.080 and 0.160 μg/μl) and LV (0.000, 0.625, 1.250, 2.500, 5.000 and 10.000 μg/μl) or BSA (0.000, 0.625, 1.250, 2.500 and 5.000 μg/μl) (Yuanye Biotechnology Co., Ltd.) in buffer comprising 0.1 mol/l NaCl and 10 mmol/l Tris-HCl at room temperature for 30 min.

In the salt-dialysis reconstitution (24), each plasmid (at a final concentration of 0.1 μg/μl) was mixed with histone octamer and LV (or BSA) in initial buffer containing 2 mol/l NaCl, 1 mmol/l EDTA and 10 mmol/l Tris-HCl (pH 7.2). The chromatin was placed into a dialysis bag (0.5 kDa; Beijing Solarbio Science & Technology Co., Ltd.) for 4 h dialysis at 8°C. Finally, the volume of the reconstituted chromatin was adjusted to 0.4 ml using buffer containing 0.1 mol/l NaCl and 10 mmol/l Tris-HCl (pH 7.2).

The samples loaded were as follows: Sample 1, 75 μl 1 mg/ml salmon sperm DNA (Beijing Solarbio Science & Technology Co., Ltd.) was incubated with 75 μl ZEL (57 mg/ml) at 4°C for 15 min, and centrifuged for 5 min at 13,400 g at 4°C. For sample 2, the supernatant of sample 1 was incubated with 7.5 μl 10 mg/ml salmon sperm DNA at 4°C for 15 min, then centrifuged for 5 min at 13,400 g at 4°C. Samples 3 and 4 were obtained via repeating this procedure. The samples were added to 40 μl Tris-HCl containing 10 μl 10% SDS and 10 μl loading buffer. Sample 5 contained 8 μl supernatant from the fourth salmon-sperm DNA precipitate mixed with 8 μl Tris-HCl, 4 μl 10% SDS and 4 μl loading buffer. Sample 6 comprised 4 μl ZEL mixed with 12 μl Tris-HCl, 4 μl 10% SDS and 4 μl loading buffer. For sample 7, 75 μl 1 mg/ml salmon-sperm DNA was mixed with 75 μl ZEL (57 mg/ml); 750 μl 0.075 mol/l NaCl was then added and the mixture was incubated at 4°C for 15 min and centrifuged for 5 min at 13,400 g. The precipitate was dissolved in 40 μl Tris-HCl containing 10 μl 10% SDS and 10 μl loading buffer. Sample 9 (histone) was prepared in the same way as sample 7 (histone) above. To generate sample 10, 175 μl FCS was incubated with 75 μl 1 mg/ml salmon-sperm DNA at 4°C for 15 min and centrifuged for 5 min at 13,400 g. This precipitate was dissolved in 40 μl Tris-HCl containing 10 μl 10% SDS and 10 μl loading buffer. Sample 11 was generated by mixing 4 μl FCS with 12 μl Tris-HCl containing 4 μl 10% SDS and 4 μl loading buffer. All samples were boiled at 100°C for 2 min. A total of 5 μl each sample was loaded onto each lane and subjected to SDS-PAGE (15% gels).

Nuclear Extraction kit (Beyotime Institute of Biotechnology) was used to extract nuclei from 20 hpf ZEs using 0.42 mol/l NaCl for two sequential extractions. Each 1 ml supernatant was mixed with 330 mg ammonium sulfate, centrifuged at 13,400 g for 5 min at 4°C and the resulting precipitate was dissolved in 0.5X Tris-EDTA (TE) buffer (10 mmol/l Tris, 1 mmol/l EDTA, pH 8.0) and loaded onto an equilibrated Sephadex G50 column (1.5×20 cm height, Pharmacia) to obtain crude RNA polymerase II for use in the following experiments.

In vitro transcription of chromatin was performed as described by You et al (26). Chromatin from deyolked 3 hpf ZEs (1,000 cells) was extracted as described by Purushothaman et al (27). The chromatin was dissolved in buffer at 4°C (0.1 mol/l NaCl and 10 mmol/l Tris-HCl; pH 7.2).

A total of 10 nmol/l C1-ORF2 recombinant (or chromatin) was incubated for 1 h at 30°C in reaction buffer with crude RNA polymerase II for 1 h at 30°C in 400 mmol/l Tris-HCl reaction buffer, which includes 200 μmol/l nucleotides, 20 U RNase inhibitor, 200 mmol/l MgCl₂, 25 mmol/l tris (2-carboxyethyl) phosphine and 20 mmol/l spermidine.

The reaction was terminated by adding 125 mmol/l Tris-HCl (pH 7.5) containing 12.5 mmol/l EDTA, 150 mmol/l NaCl, 1% SDS and 2 μg/μl protease K at 55°C for 1 h. Reverse transcription-quantitative (RT-q)PCR analysis was used to detect the mRNA levels of EZE expression genes as previously described (28). Table I shows primers for RT-qPCR analysis.

Aliquots of 20 μl LV (50 μg/μl) were injected into the abdominal cavity of adult male zebrafish (weight, 0.37-0.43 g). Total RNA was extracted from zebrafish livers 24 h after the zebrafish had been fed at 28°C in a flowthrough system. The zebrafish were submersed in water containing 100 mg/l 3-aminobenzoate methanesulfonate (Beijing Mreda Technology, Inc.) for anesthesia. The zebrafish enterocoelia were opened to obtain the zebrafish liver. Total RNA was extracted using TRIzol^® (Thermo Fisher Scientific, Inc.) from liver tissues. Total RNA was reverse-transcribed into cDNA using RevertAid First Strand cDNA Synthesis kit (Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol. Expression levels of the EZE expression genes GRHL3 (grainyhead-like transcription factor 3), SOX19A (SRY-box transcription factor 19a) and NNR (nanor) were detected using qPCR kit (cat. no. QP031, GeneCopoeia). qPCR was performed using the following thermocycling conditions: Initial denaturation at 95°C for 2 min, followed by 40 cycles at 95°C for 10 sec and 56°C for 40 sec. The 2^−∆∆Cq method was used to calculate the relative mRNA expression levels (29). The primer pairs utilized for RT-qPCR analysis are shown in Table I.

Zebrafish were placed into water containing 0.5 g/l 3-aminobenzoate methanesulfonate for ≥20 min to ensure death, prior to storage at −20°C.

RNA-seq analysis was performed by Shanghai OE Biotech. Co., Ltd., as previously reported (28). Total RNA was extracted from zebrafish liver tissue using TRIzol^®. The purity and quantification of the RNA was evaluated using a NanoDrop™ 2000 spectrophotometer (Thermo Fisher Scientific, Inc.), whereas RNA integrity was assessed using Agilent 2100 Bioanalyzer (Agilent Technologies, Inc.). Subsequently, the libraries were constructed using a TruSeq^® Stranded mRNA LT Sample Prep kit (cat. no. NR616-02, Illumina, Inc.). Gene Ontology (GO; geneontology.org/) enrichment analysis were performed.

Fragments were obtained by digesting C1-ORF2 (XhoI/PstI), C1-Alux14 (HindⅢ/NheⅠ), C1-LacZ (ApaI/XhoI) and C1 (XhoI/PstI). These fragments were precipitated with ethanol, centrifuged at 13,400 g for 5 min at 4°C and precipitate was dissolved in double distilled water. All restriction enzymes were purchased from Takara Biotechnology Co., Ltd. The final concentration of fragments was 20 ng/μl and the concentration determination method was measured by ultraviolet spectrophotometer (UV-2800A; UNICO Instrument Co., Ltd. Shanghai) at 280 nm; these fragments were incubated with histone or LV for 15 min at room temperature in 10 mmol/l Tris-100 mmol/l NaCl buffer. LV concentrations were 0.0000, 0.0625, 0.1250, 0.2500, 0.5000, 0.7500, 1.0000, 1.2500, 1.5000 and 1.7500 μg/μl in the experiments that ORF2, Alux14, C1 fragments were incubated with LV. The LV concentrations were 0.0000, 0.0125, 0.0625 and 0.3125 μg/μl and histone concentrations were 0.025 μg/μl in the experiments of the effects of incubation order. The LV concentrations were 0.0000, 0.0625, 0.1250, 0.2500, 0.5000, 1.0000 and 2.0000 μg/μl, the histone concentrations were 0.015, 0.020, 0.025, 0.030 μg/μl to assess effects of histone concentrations. A total of 10 μl of each sample was loaded into a well with the gel; all experiments were using 1.5% agarose gel with 5% ethidium bromide (cat. no.1239-45-8; Shanghai Yien Chemical Technology Co., Ltd.). Finally, images were captured using an Alpha Innotech gel-imaging analyzer (Alpha Innotech Corporation).

ChIP assay was employed to validate the affinity of LV with ORF2. ZEs (25 mg, 0 hpf) were microinjected using C1-ORF2 or C1-Alux14 (control) plasmids. Subsequently, the injected embryos were incubated at 28°C for 2 h and frozen at −20°C for processing. Samples were prepared using the SimpleChIP^® Plus Enzymatic chromatin IP kit (Cell Signaling Technology, Inc.; cat no. #9005), following the manufacturer's protocol. A total of 1.5% formaldehyde was added into the embryos for 30 min at room temperature to produce cross-linked protein and DNA and then chromatin fragments were obtained using sonication (20 sec per time; 800 Hz) at intervals of 30 sec (20 cycles) at 4°C, followed by centrifugation at 13,400 × g for 5 min at 4°C. The chromatin fragments were incubated with 0.03 μg/μl anti-LV antibody at 4°C for overnight. PCR was performed using the following EGFP primers: Forward, 5′-ACATCCTGGGGCACAAGC-3′ and reverse, 5′-CTTGTACAGCTCGTCCATGC-3′. PCR kit [cat. no. ET101, TIANGEN BIOTECH (BEIJING) CO., LTD.] was performed using the following thermocycling conditions: Initial denaturation at 94°C for 3 min, followed by 30 cycles of 94°C for 30 sec, 55°C for 30 sec and 72°C for 60 sec and final extension at 72°C for 5 min. PCR products (311 bp) were separated by 1% agarose gels and visualized using a UV transilluminator (Alpha Innotech Corp. USA).

HeLa cells (Shanghai Tongpai Biotechnology Co., Ltd.) were seeded (1×10⁵ cells/well) in 24-well plates and cultured in Dulbecco's Modified Eagle Medium (cat no. 10566016, Thermo Fisher Scientific, Inc.) with 10% fetal bovine serum (cat no. ZF181FBS-500, Zeta Life Co., Inc.) at 37°C with 5% CO₂. The cells (2×10⁵ cells/well) were transfected with C1-ORF2 vector (0.2 μg/μl) using Lipofectamine^®2000 (Thermo Fisher Scientific, Inc.) at room temperature for 5 min, following the manufacturer's protocol. After 48 h, cells were grown in selective medium containing 1 mg/ml G418 (Beijing Biotopped Life Sciences, Inc.) for approximately 3 weeks. Then, the cells stably transfected with C1-ORF2 were obtained. LV (1.18 μg/μl) was added into stably transfected HeLa cells for 48 h. Same volume saline was added into stably transfected HeLa cells as a control. ATAC-seq was performed by Shanghai Jiayin Biotechnology Ltd. using a Novaseq 6000 Sequencing System (Illumina, Inc.) as previously described (30,31). Trimmomatic software (version 0.36, usadellab.org/cms/?page=trimmomatic) was used for quality control. Burrows Wheeler Aligner-maximal exact matches software (version 0.7.13-r1126, bio-bwa.sourceforge.net/) compared the clean data to the reference (CMV-EGFP-ORF2-PolyA) (32). MACS2 software (version 2.1.2, pypi.org/project/MACS2/) was used for analysis, and Q<0.05 was used as the screening threshold. DeepTools software (3.4.3, deeptools.readthedocs.io/en/develop/) was used to analyze signal distribution near to the CMV-EGFP-ORF2-PolyA reference.

C1-OR F 2-h istone-LV a nd C1-Alux14-histone-LV recombinants were obtained by the incubation reconstitution (see subsection: In vitro chromatin reconstitution). The recombinants were digested with 0.045 U/μl DNase Ⅰ for 0 sec, 30 sec, 2 min or 4 min at room temperature. Next, the recombinants of C1-ORF2-histone-LV and C1-ORF2-histone-BSA were obtained using the dialysis recombination. Briefly, 100 μl of four different recombinant solutions were digested with DNase I (0.02, 0.04 or 0.08 U/μl) at room temperature for 1 min. Aliquots 10 μl termination solution (0.1 % SDS-10 mmol/l EDTA) was added and then precipitated with absolute ethyl alcohol. The precipitates were washed twice with 75% ethanol, dried, dissolved with 50 μl 2.5% SDS and 1/10 volume of xylene cyanol FF loading buffer. Each 10 μl sample was loaded into one lane and subject 1.5% agarose gel electrophoresis.

Each experiment was repeated at least three times. Data are presented as the mean ± standard deviations (SD). Statistical analysis was performed using SPSS software (version 17.0; IBM Corporation) and GraphPad Prism (version 6.0; Dotmatics). Group differences were assessed using one-way ANOVA with Tukey's post hoc test. P<0.05 was considered to indicate a statistically significant difference.

To determine whether human L1-ORF2 enhances EGFP expression in EZEs, C1-ORF2, C1-Alux14, C1-LacZ and pEGFP-C1 (C1) expression vectors were injected into 0 hpf ZEs and subsequently the EGFP fluorescence intensity was observed at 24 h post-injection. Brightest EGFP fluorescence was observed in the C1-ORF2 group (Fig. 1A and B). C1-ORF2 was injected into 0 hpf ZEs and the EGFP fluorescence intensity was observed at 6, 12, 24 and 48 h post-injection. EGFP fluorescence intensity induced by C1-ORF2 increased with time (Fig. 1C and D). However, when C1-ORF2 was injected into 0, 2 and 4 hpf ZEs, EGFP fluorescence intensity of 0 hpf was higher than of 2 hpf and 4 hpf groups, which indicated that EGFP expression is related to embryo development stage (Fig. 1E and F). Taken together, these results suggested that the developmental stage affected expression of EGFP induced by C1-ORF2 in EZEs. To determine whether ORF2 activates EGFP via transcriptional changes, RT-qPCR was used to quantify EGFP mRNA. C1-ORF2 significantly increased expression of EGFP mRNA compared with C1-Alux14 or C1-LacZ vectors (Fig. 1G). These results suggested that ORF2 could activate EGFP gene expression at the transcriptional level.

To exclude any enhancer role of poly(A) on EGFP activation, poly(A) was removed from the C1 plasmid, generating C1-delPolyA. The C1, C1-ORF2, C1-delPolyA, C1-delPolyA-ORF2 and C1-delPolyA-ZORF2 vectors were injected into EZEs and the lowest EGFP fluorescence intensity was observed in the C1-delPolyA group, whereas the EGFP fluorescence intensity induced by C1-delPolyA-ORF2 and C1-delPolyA-ZORF2 were significantly higher compared with that induced by C1-delPolyA (Fig. 1H and I). These results further demonstrated that ORF2 activated EGFP gene expression in EZEs.

To observe the effects of histone on ORF2-induced EGFP expression in EZEs, C1-ORF2 was incubated with histone and injected into 0 hpf ZEs. EGFP expression was then observed at 24 h post-injection. EGFP fluorescence decreased as histone concentration increased (Fig. 2A). Upon incubation with 0.04 μg/μl histone, the intensity of EGFP induced by ORF2 decreased by almost 50% compared with 0 μg/μl histone (Fig. 2B).

Based on relative levels of histones and transcription factors, which both regulate the onset of transcription in the EZEs (33), it was hypothesized that ZEL contains certain components that eliminate the inhibitory effect of histones on C1-ORF2. As the concentration of ZEL increased, the inhibitory effect induced by histones decreased (Fig. 2D); 3.8 μg/μl ZEL could eliminate 80.49% of the histone-mediated inhibition of EGFP expression (Fig. 2C). These findings indicated that ZEL attenuates the suppression of ORF2-dependent EGFP expression by histone.

It was hypothesized that DNA-binding proteins of the ZEL could activate EGFP fluorescence via interaction with C1-ORF2 in 0 hpf ZEs. Salmon sperm DNA was incubated with ZEL and the key proteins were divided according to their molecular mass (~115, ~100 and ~25 kDa; Fig. 3A and B).

LV was purified from ZEL. The purified LV was analyzed using Easy-nLC1200 high-performance liquid chromatography (Table SI). The different concentrations of LV (0, 0.625, 1.25, 2.5, 5.0 and 10 μg/μl) were incubated with histone and C1-ORF2. LV could attenuate the inhibitory effect of histone on C1-ORF2-induced EGFP expression (Fig. 3C and D); by contrast, BSA failed to alleviate the inhibitory effect of histone on EGFP expression at any concentration (Fig. 3E).

MZP, which does not contain LV, was used as an appropriate control for demonstrating the specificity of LV. MZP was found not to attenuate histone-induced inhibition on EGFP expression (Fig. 4A and B). Globin is an abundant protein in MZP, with a molecular weight of ~13 kDa (34,35). SDS-PAGE showed that globin was one of the abundant proteins in MZP (Fig. 4C). Different concentrations of globin did not weaken histone-induced inhibition (Fig. 4D and E).

In a previous study, the concentration of LV was higher in good-compared with poor-quality eggs (36). To explore the role of LV in EGFP gene activation, C1-delPolyA, C1-delPolyA-ORF2 and C1-delPolyA-ZORF2 were injected into 0 hpf ZEs with poor or good quality, and EGFP fluorescence was observed at 24 h post-injection. ORF2 and ZORF2 could induce strong EGFP fluorescence in good-but not in poor-quality embryos (Fig. 5A and B).

An in vitro transcription assay was employed to explore whether LV serves a role in gene expression regulation. Histone inhibited EGFP transcription, whereas LV attenuated this inhibitory effect (Fig. 5C). LV increased the mRNA levels of the GRHL3, SOX19A and NNR (Fig. 5D).

To verify whether results were reflective of the role of LV in terms of regulating transcription of ZEs, LV was injected into the abdominal cavity of adult male zebrafish. RT-qPCR was then used to detect the expression levels of the GRHL3, SOX19A and NNR genes. LV could increase transcription of the GRHL3, SOX19A and NNR genes (Fig. 5E). Furthermore, RNA-seq method was used to detect the influence of LV on the gene expression profile of liver tissue. LV increased the transcription of SOX19A by 4.89-fold; RT-qPCR shows that LV increased the transcription level of SOX19A by 2.73-fold (Fig. 5E). However, GRHL3 and NNR genes were not detected by RNA-seq. Sensitivity of RNA-seq is lower than that of RT-qPCR (35). GO enrichment analyses showed that the upregulated genes induced by LV injection were significantly enriched in 'cell development' (Fig. 5F). These results demonstrated that LV increased the expression of genes associated with early embryo development.

As LV is primarily found in the yolk sac of embryo, it was important to ensure that LV could move into cell nucleus. FITC-LV was injected into the animal pole or yolk sac of ZEs at 0 or 3 hpf and fluorescence was observed after 72 h. When FITC-LV was injected into the animal pole, green fluorescence was found in both zebrafish and cells, including the nucleus. This indicated that FITC-LV could cross the zebrafish cell and nuclear membrane (Fig. 6A and C). When FITC-LV was injected into the yolk sac of zebrafish embryo at 0 hpf, both zebrafish and cells (including nuclei) showed green fluorescence (Fig. 6B). However, when FITC-LV was injected into yolk sac of 3 hpf embryos, the fluorescence was only found in yolk sac (Fig. 6D). These findings indicated that FITC-LV was unable to penetrate the syncytial layer at 3 hpf of embryonic development.LV was passed through the cell and nuclear membrane and might therefore have an important role in early embryos.

Since LV serves an important role in gene regulation, the present study explored which DNA fragment best binds LV. ChIP analysis of the embryo tissue revealed LV bound ORF2 more readily than it did Alux14 (Fig. 7A). In addition, ORF2, Alux14 and C1 fragments were incubated with LV. EMSAs showed that the binding ability of ORF2 and LV was greater compared with that of LV with C1 or Alux14 (Fig. 7B and C).

LV could ameliorate the inhibitory effect on C1-ORF2 mediated by histone, To determine the underlying mechanism, histone, C1/ORF2 fragments and LV were mixed. Histone was incubated with LV and C1/ORF2 fragments. EMSA showed that C1/ORF2 fragments underwent complete hysteresis at 0 μg/μl LV (Fig. 8A, lane 2). With increasing LV concentrations (0.0125 and 0.0625 μg/μl), both C1 and ORF2 underwent partial gel shifts (Fig. 8A; lanes 3 and 4); but when LV concentration was high (0.03125 μg/μl), the C1 and ORF2 fragments underwent complete shifts (Fig. 8A, lane 5). When C1/ORF2 fragments were incubated with histone first and subsequently with LV, all concentrations of LV caused complete gel retardation of the C1 and ORF2 fragments (Fig. 8A). Similarly, when C1/ORF2 fragments were incubated with LV first and with histone, all concentrations of LV caused complete gel retardation of the C1 and ORF2 fragments (Fig. 8A). Fig. 8B shows the sum of the IOD values of the C1 and ORF2 fragments in each lane. Subsequently, effects of histone concentration on gel retardation when histone was incubated with LV prior to addition of C1/ORF2 were examined. LV induced the partial shift of C1/ORF2 with 0.015 μg/μl, 0.02 and 0.025, but not 0.03 μg/μl histone (Fig. 8C and D).

Transcription factors act on specific regions of chromatin to improve chromatin accessibility, manifested as an increased sensitivity to DNase I digestion (37). The present study investigated whether LV was able to promote the sensitivity of C1-ORF2 to DNase I digestion. C1-ORF2 DNA was more easily digested compared with C1-Alux14 (Fig. 9A and B). LV or BSA was incubated with C1-ORF2 and histone by salt-dialysis reconstitution and digested with different concentrations of DNase I. The brightness of the C1-ORF2 fragments incubated with LV was significantly lower compared with BSA when digested using the same concentration of DNase I (Fig. 9C and D). Taken together, these results suggested that LV promoted sensitivity of C1-ORF2 to DNase I digestion, which indicated that LV increased the chromatin accessibility of C1-ORF2 recombinant.

To verify that LV was able to improve chromatin accessibility of the cytomegalovirus (CMV) region (enhancer and promoter) of the EGFP gene in the C1-ORF2 plasmid, HeLa cells were stably transfected with C1-ORF2 plasmid and treated with LV. ATAC-seq was performed to measure the degree of chromatin opening in the CMV region of the EGFP gene in stably transfected plasmids. There were more CMV-area ATAC-seq signals in the LV compared with the control group (Fig. 9E and F). Taken together, the results of ATAC-seq confirmed that LV enhanced the CMV chromatin accessibility of C1-ORF2, consistent with the DNase I digestion experiments.