The role of nuclear localization signal in parvovirus life cycle
© The Author(s). 2017
Received: 3 January 2017
Accepted: 29 March 2017
Published: 14 April 2017
Parvoviruses are small, non-enveloped viruses with an approximately 5.0 kb, single-stranded DNA genome. Usually, the parvovirus capsid gene contains one or more nuclear localization signals (NLSs), which are required for guiding the virus particle into the nucleus through the nuclear pore. However, several classical NLSs (cNLSs) and non-classical NLSs (ncNLSs) have been identified in non-structural genes, and the ncNLSs can also target non-structural proteins into the nucleus. In this review, we have summarized recent research findings on parvovirus NLSs. The capsid protein of the adeno-associated virus has four potential nuclear localization sequences, named basic region 1 (BR), BR2, BR3 and BR4. BR3 was identified as an NLS by fusing it with green fluorescent protein. Moreover, BR3 and BR4 are required for infectivity and virion assembly. In Protoparvovirus, the canine parvovirus has a common cNLS located in the VP1 unique region, similar to parvovirus minute virus of mice (MVM) and porcine parvovirus. Moreover, an ncNLS is found in the C-terminal region of MVM VP1/2. Parvovirus B19 also contains an ncNLS in the C-terminal region of VP1/2, which is essential for the nuclear transport of VP1/VP2. Approximately 1 or 2 cNLSs and 1 ncNLS have been reported in the non-structural protein of bocaviruses. Understanding the role of the NLS in the process of parvovirus infection and its mechanism of nuclear transport will contribute to the development of therapeutic vaccines and novel antiviral medicines.
KeywordsParvovirus Nuclear localization signal Nuclear transport
Parvoviruses are the smallest animal DNA viruses and constitute a widely dispersed virus family. They infect a wide variety of hosts, including insects, birds, and mammals. The family Parvoviridae is divided into two subfamilies, the Parvovirinae and the Densovirinae. The former infects vertebrates, while the latter infects invertebrates. Through phylogenetic analyses based on DNA and protein sequences, the subfamily Parvovirinae has been divided into eight genera: Amdoparvovirus, Aveparvovirus, Bocaparvovirus, Copiparvovirus, Dependoparvovirus, Erythroparvovirus, Protoparvovirus, and Tetraparvovirus. Human parvovirus B19, belonging to the genus Erythroparvovirus, is a prominent human pathogen and causes severe syndromes in pregnant women and in individuals with underlying immune or haematologic disorders, such as hydrops foetalis and arthropathy . The adeno-associated virus (AAV), a member of Dependoparvovirus, is non-pathogenic, and its infection and replication depend on helper viruses, such as adenoviruses . Moreover, AAV is a vital gene therapy vector for human application. The bocavirus is classified in the genus Bocaparvovirus and can be detected in humans , cattle [4, 5], and other species. The human bocavirus is prevalent among children and can cause respiratory tract infections . In animals, several parvoviruses, such as goose parvovirus , canine parvovirus , and bovine parvovirus , can cause enteritis and diarrhoea.
Parvoviridae is a family of 5-kb single-stranded DNA viruses with a non-enveloped capsid . At both terminals, the linear, single-stranded genome contains palindromic sequences forming inverted terminal repeats, which can form a hairpin structure. The inverted terminal repeats provide most of the cis-acting information, which is required for both viral DNA replication and encapsidation . There are two open reading frames (ORFs) in the viral genome. The left ORF, ORF1, encodes non-structural (NS) proteins, while the right ORF, ORF2, encodes two or three viral structural proteins. However, the Bocaparvovirus has an extra ORF located between ORF1 and ORF2 that encodes the non-structural protein (NP) 1 [12, 13]. The NS protein is a replicate protein needed for viral genomic replication  and works as a cytotoxic protein leading to apoptosis of host cells . Generally, the virion is composed of two or three capsid proteins (VP1-VP3) which share an identical C-terminal sequence. The VP1 sequence comprises the entire VP2 sequence and an ~140 amino acid N-terminal extension called VP1 unique region (VP1u). The VP1u, especially the phospholipase A2 (PLA2) domain and the nuclear localization signal (NLS) located in the unique N terminus of VP1, is necessary for infectivity . The PLA2 domain is required for parvovirus infectivity [17, 18], while the NLS plays an important role in the parvovirus replication cycle [19, 20]. In the early steps of infection, the NLS assists the translocation of viral genomes to the nucleus, whereas in the late steps of infection, the NLS is required for nuclear transport of viral capsid proteins.
NLSs are usually composed of basic residues (K and R), tend to be hydrophilic, and are divided into classical (cNLS) and non-classical (ncNLS) types. The cNLSs are further divided into classical monopartite NLS and classical bipartite NLS. In the cytoplasm, the small proteins can be transported into the nucleus through the nuclear pore complex freely or by passive diffusion, while the larger proteins (>50 kDa) require active transport. Large proteins can be transported into the nucleus with the help of an NLS . Notably, the functions of NLSs have been identified in some DNA viruses, such as herpesvirus [22, 23], circovirus [24, 25], as well as some RNA viruses [26, 27]. An NLS identified in the herpesvirus VP1/2 capsid protein is important for infection via capsid routing to the nuclear pore complex . Furthermore, an NLS found in the polymerase of the borna disease virus is essential for targeting this polymerase into the nucleus . Several ncNLSs and cNLSs, which can guide the capsid protein into the nucleus and play a role in virus infection, have been identified in the structural proteins of parvoviruses. In this paper, based on the latest research progresses, we summarize the current knowledge about the role of NLSs in the parvovirus replication cycle, which may help us to better understand the molecular pathogenesis of parvoviruses.
The NLS of parvoviruses
The NLS of Dependoparvovirus
The NLS of Protoparvovirus
A BR of the canine parvovirus (CPV) capsid protein sequences has been analysed, and it has basic amino acids (K and R) common with most of the previously identified nuclear localization signals (Fig. 1b i). Based on that information, one peptide (PAKRARRGYKC) of the BR1 was synthesized and subsequently was conjugated with bovine serum albumin. The conjugates were labelled with rhodamine B and microinjected into the cytoplasm of A72 cells. Notably, the BR1 containing the N-terminal region (aa 4PAKRARRGYK13) of CPV was capable of efficiently transporting bovine serum albumin into the nucleus of A72 cells at 60 min post-injection . Therefore, the BR1 (4PAKRARRGYK13) located in the CPV VP1 capsid protein was identified as having NLS functions. Another study using glycine scanning mutagenesis indicated that lysine at position 6 and two arginines at positions 7 and 9 of the VP played important roles in its nuclear targeting activity . Subsequently, an infectious clone of CPV was constructed to generate mutated recombinant virus. When Lys 6, Arg 7, and Arg 9 of the CPV VP were substituted by Ala, the infectivity of the virus was diminished. Therefore, the BR1 is essential for viral infectivity. Interestingly, the infectivity of virus was not affected by single substitution of either Lys 6 or Arg 7 of CPV with Ala, showing titre levels similar to the wild-type CPV . Although the motif 4PAKRARRGYK13 was identified as the NLS of CPV, its role in the early steps of infection when viruses deliver their genomes into the nucleus for replication and transcription, as well as in the late steps of infection when progeny viral capsid subunits are transported into the nucleus for assembly into progeny virions, was largely unknown.
A nuclear localization motif (NLM) and four BRs were found in the capsid protein of parvovirus minute virus of mice (MVM). The NLM is located in the overlap region of VP1/VP2, while the BRs are found in the N-terminus of VP1 [19, 33]. Moreover, a bipartite cNLS, which was found in the position 194 to the 216 of NS1 protein gene (194KK[X]18KKK216), is essential for translocation of NS1 into the nucleus . The NLM (528KGKLTMRAKLR538) is composed of five basic amino acids (K and R) in the C-terminal residues of VP1/VP2 and located in a beta-sheet (Fig. 1b ii). The four BRs, called BR1 (6KRAKR10), BR2 (87RTKR90), BR3 (109RAGKRTRPP117), and BR4 (126RAKKK130), are highly conserved among parvoviruses (Fig. 1b ii). Different BRs play different roles in viral protein localization [19, 33]. By constructing a series of contiguous and overlapping deletion mutants, two major nuclear localization regions, BR1 and NLM, were confirmed as being involved in the accumulation of VP1 in the nucleus of infected cells. However, the MVM BR2 behaved as a weak NLS, while BR3 and BR4 lacked NLS activity . In addition, the NLM is necessary for the nuclear localization of MVM VP2 protein and displays nuclear localization activity for VP subunits. The nuclear location of MVM-VP plasmid with the NLM and without BRs was identified, suggesting that the NLM plays an important role in the late steps of infection leading to progeny viral capsid subunits entering the nucleus [19, 33]. Moreover, NB324K cells were transfected with an infectious MVM plasmid with all BR sequences mutated or deleted, and the result suggested that all BR sequences were not essential for the nuclear translocation of the progeny viral capsid subunits [19, 33]. However, the mutant virions showed lower infectivity than WT virions, which indicated that the BR sequences may play an important role in the early steps of the infection process. Considering the PLA2 domain is located between BR1 and BR2, a mutation or deletion in BR1 and BR2 may have an influence on the activity of phospholipase. Thus, the specific function of the BR sequence should be further studied.
Five BRs were found in the VP1u of porcine parvovirus (PPV), named BR1 (3PPAKRAR9), BR2 (86RAKR89), BR3 (110RRSPRK115), BR4 (124KR125), and BR5 (133KKKAK137)  (Fig. 1b iii). Both BR1 and the combination of BR4 and BR5 (BR4-5) were cNLSs, and the BR4-5 was a bipartite NLS. BR1 and BR4-5 were required for the onset of infection . To investigate the NLS activity of PPV BRs, each of the BRs with EGFP tag was expressed in eukaryotic porcine fibroblast cells. EGFP-BR1 and EGPF-BR4-5 fused proteins were almost exclusively localized in the nucleus of cells, indicating the NLS activity of the BR1 and BR4-5. However, the EGFP-BR2 and EGFP-BR3 were only slightly accumulated in the nucleus of cells. Furthermore, a recombinant PPV infection clone, with the PPAKRAR sequence of BR1 and the KKKAK of BR4-5 substituted by neutral hydrophilic polar amino acids (such as Asn, Thr, and Gln), was constructed and used to transfect porcine fibroblast cells. Consequently, no infectious virus was rescued . Interestingly, the infectious virions, which had lower infectivity than WT virus, could be rescued when the infection clone had only BR1 or BR4-5 mutated . These results indicate that the BR1 and BR4-5 play an important role in the PPV infectious cycle. Moreover, three potential regions of NLM were identified in the capsid of PPV, including an external region (containing of R374, R393, and R565) on the surface of the assembled capsid, a central region (containing of K475, R477) in the interior region of the trimer, and an internal region (containing of K272, K275, K487, R533, K535, R576) in the interior face of the capsid . Mutation experiments confirmed that K275 and R533 were important for nuclear targeting of PPV VP2. Any mutagenesis of single amino acid at K275 or R533 was able to block the transport of VP2 into the nucleus, which indicates that the internal region is the NLM of PPV. Similar to the NLM of MVM, the NLM of PPV is needed for the correct folding of the protein and is responsible for translocation of VP2 into the nucleus. Collectively, the BR1 and BR4-5, located in the VP1 N-terminus of PPV, can assist the localization of the virus to the nucleus during the early steps of infection after the exposure of the VP1 N-terminus or at the late steps of infection when the capsid subunits are transported to the nucleus. However, the functions of NLSs and potential NLMs of PPV in the infection process need to be further illustrated.
The NLS of Erythroparvovirus
An ncNLS was identified and located in the C-terminal region of the human parvovirus B19 major capsid protein VP2 (Fig. 1c). The sequence, 720KLGPRKATGRW730, is necessary for nuclear targeting of VP2 . It is conserved among the C-terminal region of erythrovirus VP2 proteins. Interestingly, no cNLS was predicted in B19 VP2 capsid protein by using the PSORT II program. The major capsid protein VP2 of parvovirus B19 was located in the nucleus of primary erythroid cells by using indirect immunofluorescence analysis . To find the nuclear localization signal of B19 VP2 capsid protein, the localization of full-length VP2 (aa VP 228-781) protein and a C-terminal, truncated form of VP2 (aa VP 228-670) were analysed by using indirect immunofluorescence, which showed that the C-terminal, truncated VP2 protein aberrantly remained in the cytoplasm of transfected COS-6 cells. Subsequently, three clusters of basic residues included between amino acid 720 and 781 were found. Then, the KLGPRKATGRW sequence (aa VP 720-730) was fused into pEGFP-C1, and the fluorescence signal was detected in the nucleus of transfected COS-6 cells . Further experiments indicated that this sequence is also capable of transporting β-galactosidase fusion protein into the nucleus, confirming its importance in nuclear transport . Although its function has been identified, the role of this sequence in the replicative cycle of erythroviruses is still unclear and thus, should be confirmed by constructing a B19 infection clone.
The NLS of Bocaparvovirus
The non-structural protein (NP) 1 of human bocavirus (HBoV), which is encoded by the third open reading frame, is critical for the expression of the viral capsid protein. Jianming Qiu et al. found that NP1 is required for maturation of the capsid protein-encoding mRNA . However, other non-structural proteins are not necessary for the expression of HBoV VP1/VP2/VP3. A classical bipartite NLS (cNLS aa 14–28) and an ncNLS (aa 7–50) were found in the N-terminal region of the NP1 gene (Fig. 1d i), both of which can transport a heterologous large cytoplasmic protein, β-galactosidase fusion protein, into the nucleus . Moreover, two cNLSs (cNLS1 aa 52–58 and cNLS2 aa 60–66) and an ncNLS (aa 1–51) were identified in the N-terminal region of porcine bocavirus (PBoV) NP1 protein  (Fig. 1d ii). Amongst these, the two cNLSs have stronger nuclear transport ability than the ncNLS. Notably, this N-terminal region can inactivate the promoter activity of interferon β . Although the NLSs were identified in NP1 of HBoV and PBoV, whether the capsid proteins also contain the NLS is unknown and remains to be studied.
Parvoviruses are DNA viruses, which bind to the receptor of host cell surface upon infection and are subsequently internalized into the cytoplasm, following which they get into the nucleus with the guidance of the NLS and replicate and assemble in the nucleus of host cells. In the process of infection, the NLS is required for the virion life cycle, especially for the nuclear import of progeny viral proteins. In this review, we summarized the roles of the NLS in the parvovirus life cycle. However, the interaction between the functional NLS of parvovirus and importin of the host is still unknown. Accordingly, a thorough understanding of the mechanisms of the interplay between the NLS of parvovirus and the importin of the host may contribute to the development of antiviral vaccine candidates and novel inhibitors.
Human parvovirus B19
Classical nuclear localization signal
Minute virus of mice
Non-classical nuclear localization signal
Nuclear localization motif
Nuclear localization signal
- PLA2 :
VP1 unique region
This work was funded by grants from Innovative Research Team Program in Education Department of Sichuan Province (No.2013TD0015), the National Science and Technology Support Program (2015BAD12N05), the Integration and Demonstration of Key Technologies for Duck Industrial in Sichuan Province (2014NZ0030), and China Agricultural Research System (CARS-43-8).
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Peng Liu and Shun Chen developed the structural design of the review and drafted the manuscript. Mingshu Wang and Anchun Cheng were involved in revising the manuscript critically for important intellectual content. All author read and approved the final manuscript.
The authors declare that they have no competing interests.
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