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Editorial note: see also the reviews of the related gene in the same species in <../AcrF8/AcrF8-deep-research.md>
Transcriptional Repressor of Anti-CRISPR Operon: The ACA2 gene encodes the anti-CRISPR associated protein Aca2, a small DNA-binding regulator that represses the expression of the adjacent anti-CRISPR gene. In phage ZF40 (a temperate bacteriophage of Pectobacterium carotovorum), Aca2 forms a homodimer and binds specifically to an inverted repeat operator sequence in the acrIF8–aca2 operon promoter (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). By binding overlapping the −35/−10 elements of the promoter, Aca2 blocks RNA polymerase recruitment, thereby shutting off transcription of the anti-CRISPR gene (acrIF8) and its own gene in an autoregulatory feedback loop (pmc.ncbi.nlm.nih.gov). This negative feedback ensures that anti-CRISPR (AcrIF8) protein is produced immediately upon infection to disable the host’s CRISPR-Cas immunity, but is then quickly downregulated once the phage genome is secured in the cell (www.nature.com) (pmc.ncbi.nlm.nih.gov). Aca2’s action exemplifies an “anti-anti-CRISPR” mechanism: it counteracts the phage’s own anti-CRISPR protein to fine-tune the level and timing of host immune suppression (pmc.ncbi.nlm.nih.gov).
Dual DNA and RNA Binding Mechanism: Recent evidence revealed that Aca2 is a bifunctional regulator affecting gene expression at two levels. In addition to its role as a transcriptional repressor, Aca2 binds directly to a conserved stem-loop structure in the acrIF8–aca2 mRNA, blocking ribosome access and thus inhibiting translation of the anti-CRISPR protein (www.nature.com). Cryo-EM structural analysis showed the helix-turn-helix (HTH) domain of Aca2 engaged with RNA, demonstrating how the same HTH motif can specifically recognize RNA secondary structure as well as DNA operator sites (www.nature.com). Through this dual control—transcriptional repression via DNA binding and translational repression via RNA binding—Aca2 adjusts anti-CRISPR production in response to increasing phage genome copy number and accumulating acr mRNA (www.rcsb.org). This combined mechanism allows the phage to suppress the host CRISPR-Cas defense efficiently while preventing toxic overexpression of the AcrIF8 inhibitor protein (www.rcsb.org). In summary, Aca2’s molecular function is a sequence-specific DNA/RNA-binding repressor that tightly regulates anti-CRISPR gene expression at multiple levels.
Intracellular (Bacterial Host Cytoplasm/Nucleoid): Aca2 is a phage-derived protein that functions inside the Pectobacterium host cell during infection. It is not a structural component of the phage particle, meaning no Aca2 protein is packaged in the virion; instead, the aca2 gene is expressed after the phage genome is injected or excised into the host (pmc.ncbi.nlm.nih.gov). Once expressed in the bacterial cytoplasm, Aca2 proteins diffuse and bind to the phage operon’s DNA, which resides either on the injected phage DNA (during lytic infection) or in the integrated prophage within the bacterial chromosome (during lysogeny). Thus, Aca2 localizes to the host nucleoid region, associating with the phage operon’s promoter DNA as part of a repressor complex. Consistent with its role as a DNA-binding transcription factor, Aca2 operates in the bacterial intracellular space, likely concentrated at the phage operon’s operator site on DNA. It may also interact with target mRNA in the cytosol (given its RNA-binding activity), but it does not have any membrane association or secretory signal. In GO terms, Aca2 would be placed in the host cell cytoplasm or nucleoid (cellular component), reflecting that it functions within the infected bacterium’s cell to bind nucleic acids and is not found outside the host cell (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov).
Phage Immune Evasion and Lifecycle Regulation: Aca2 is centrally involved in the bacteriophage’s strategy to overcome and then coexist with the host’s immune system. Upon phage infection, rapid expression of anti-CRISPR (acr) genes like acrIF8 allows the virus to evade the host’s CRISPR-Cas defense (www.nature.com). Aca2 then represses the acrIF8–aca2 operon, presumably to reduce fitness costs to the host and phage once the immediate need for CRISPR suppression has passed (www.nature.com). This regulation is crucial during the transition from the lytic infection phase to lysogeny (prophage establishment): high AcrIF8 levels early on protect the phage DNA from CRISPR interference, but as the phage establishes a stable lysogenic state, Aca2 curtails further Acr production (pmc.ncbi.nlm.nih.gov). By fine-tuning anti-CRISPR levels, Aca2 facilitates successful integration and maintenance of the prophage without killing the host or inducing unnecessary immune stress (pmc.ncbi.nlm.nih.gov). In effect, Aca2 participates in viral latency establishment and the regulation of phage life cycle. It acts at the interface of viral and host processes: promoting phage survival by transiently blocking host immunity, then allowing normal host cell function to resume to support the dormant phage.
Regulation of Gene Expression: At the molecular level, Aca2 is involved in several gene regulatory processes. It is a key player in negative regulation of transcription, DNA-templated – specifically repressing the acrIF8-aca2 operon’s transcription by binding its promoter (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). It also contributes to negative regulation of translation, by directly binding mRNA to prevent protein synthesis (a rarer function for a phage HTH protein) (www.nature.com). These activities position Aca2 as a critical node in controlling gene expression timing and levels during phage infection. Functionally, it ensures that anti-CRISPR protein production is transient and appropriately scaled: enough to neutralize host defenses, but not so much as to incur cellular toxicity or hinder later phage processes (www.rcsb.org). Indeed, Aca2-mediated repression is crucial for phage ZF40 replication, as loss of this regulation leads to unrestrained acrIF8 expression that compromises the phage’s ability to propagate (www.jbc.org). Overall, Aca2 is intimately involved in the biological processes of viral defense evasion modulation, phage development, and transcriptional/translational control within the host.
Plant Pathogen Context: Pectobacterium carotovorum (formerly Erwinia carotovora) – the host of phage ZF40 – is a phytopathogenic bacterium that causes soft-rot diseases in various plants (notably potatoes and other vegetables) (pmc.ncbi.nlm.nih.gov). While the ACA2 gene is not directly associated with a human disease, it is relevant in the context of plant disease because it influences the interactions between phage and this plant pathogen. The presence of the acrIF8-aca2 operon in phage ZF40 may impact the bacterium’s ability to evade or withstand certain defenses. For instance, acrIF8 enables the phage (and any lysogenized host) to overcome Pectobacterium’s or related species’ type I-F CRISPR-Cas immune systems (pmc.ncbi.nlm.nih.gov). This can affect the success of phage infection and lysogeny in strains that have active CRISPR defenses (such as P. atrosepticum, another plant pathogen with type I-F CRISPR) (pmc.ncbi.nlm.nih.gov). There is no evidence that Aca2 contributes to virulence of the bacterium directly; rather, its role is specific to phage genetic regulation and immunity evasion.
Phenotypic Consequences of Aca2 Manipulation: Experimental studies have shown that Aca2 is essential for phage viability in the lytic cycle. Deletion of the aca2 gene from the ZF40 phage genome results in non-viable phage – the mutant phages cannot successfully complete lytic replication (www.jbc.org). This lethal phenotype is due to dysregulation of the anti-CRISPR: without Aca2, the acrIF8 gene is constitutively expressed, which severely compromises phage replication (www.jbc.org). The unregulated, high levels of AcrIF8 not only fail to improve phage survival, but actually prove toxic to the bacterial host as well, likely by over-inhibiting critical host processes or triggering cellular stress (www.jbc.org). Indeed, overexpression of AcrIF8 in Pectobacterium was shown to inhibit bacterial conjugation efficiency, indicating a fitness cost to the host when Acr is excessive (www.jbc.org). Thus, Aca2’s regulatory function is required to prevent such detrimental outcomes. In summary, the key phenotype associated with Aca2 is its requirement for normal phage replication and lysogeny: phages lacking Aca2 cannot propagate, and hosts with runaway AcrIF8 expression suffer growth and function defects. These findings underscore Aca2’s role in balancing phage-host interactions – too little AcrIF8 and the phage is eliminated by CRISPR, too much and the host (and thereby the phage’s niche) is harmed (www.rcsb.org) (www.jbc.org). By maintaining this balance, Aca2 indirectly influences the persistence of the phage in bacterial populations, which could in turn affect the epidemiology of the plant disease (since lysogeny can potentially modulate bacterial virulence or immunity, though no direct disease phenotype is attributed to Aca2 itself).
Helix-Turn-Helix (HTH) DNA-Binding Domain: Aca2 is a relatively small protein (≈116 amino acids) that belongs to the helix-turn-helix family of DNA-binding proteins (pmc.ncbi.nlm.nih.gov). The N-terminal region (approximately residues 1–70) forms a classical HTH domain, comprising multiple α-helices of which helix α3 serves as the recognition helix that fits into the major groove of DNA (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). This domain architecture is characteristic of many prokaryotic transcriptional repressors. In Aca2, two conserved helices (α2–α3) form the HTH motif that mediates sequence-specific binding to the operator DNA inverted repeat (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). Several key residues within the HTH (identified by mutational analyses) are highly conserved among Aca2 homologs, underscoring the functional importance of this DNA-binding motif (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). Structural comparisons have noted that Aca2’s HTH domain is structurally analogous to those found in other bacterial transcription factors; for example, it superimposes with the HTH of E. coli MqsA (a DNA-binding antitoxin repressor) despite low sequence identity (pmc.ncbi.nlm.nih.gov). This highlights the evolutionary reuse of HTH folds in diverse regulators.
C-terminal Dimerization Interface: Unlike the smaller Aca1 family proteins (~70 amino acids), Aca2 contains a C-terminal extension beyond the HTH domain (residues ~71–116) that is critical for its dimerization and regulatory function (pmc.ncbi.nlm.nih.gov). Each Aca2 protein monomer has six α-helices in total and two β-strands; the C-terminal helices and β-strands (sometimes referred to as the C-terminal domain, CTD) mediate inter-subunit interactions in the Aca2 homodimer (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). Crystal structures of Aca2 show that it forms a rigid homodimer: the two monomers associate in an antiparallel fashion, where the C-terminal β1–α5–α6–β2 region of one protomer packs against the N-terminal helix (α1) of the other protomer, and vice versa (pmc.ncbi.nlm.nih.gov). This intertwined dimer interface is held together by a network of hydrophobic contacts and salt bridges (e.g., involving conserved residues like Glu5 at the N-terminus and Tyr108 in the C-terminus) (pmc.ncbi.nlm.nih.gov). The dimerization surface is well-conserved across Aca2 family members, indicating that forming a dimer is an intrinsic and functionally required feature of these proteins (pmc.ncbi.nlm.nih.gov). Dimerization is in fact essential for DNA binding – each Aca2 dimer presents two HTH motifs, which together engage the symmetric half-sites of the operator’s inverted repeat. Mutations that disrupt the dimer interface (for example, E5A/Y108A double mutant) abolish dimer formation and thereby eliminate DNA binding and repressor activity (pmc.ncbi.nlm.nih.gov). In summary, Aca2’s domain structure can be viewed as bipartite: an N-terminal HTH DNA-binding domain and a C-terminal dimerization domain. This arrangement allows Aca2 to function as a dimeric, DNA/RNA-binding repressor. Notably, Aca2 does not contain any enzymatic domains or known ligand-binding pockets – its function is executed purely through protein–nucleic acid interactions via these structural motifs. Consistent with a transcription factor, Aca2 lacks signal peptides or membrane spans; it is a soluble, nucleic-acid-binding protein.
Operon Structure and Autoregulation: The aca2 gene is co-transcribed with the upstream anti-CRISPR gene (acrIF8) in a single operon, under control of the acrIF8–aca2 promoter (pmc.ncbi.nlm.nih.gov). This operon organization is key to Aca2’s regulatory dynamics. During initial phage infection (or prophage induction), the acrIF8-aca2 promoter is activated, resulting in a burst of transcription that produces both AcrIF8 and Aca2 proteins. AcrIF8, being the first cistron, is produced immediately to inhibit host CRISPR defenses, while Aca2 protein accumulates slightly later from the same mRNA (pmc.ncbi.nlm.nih.gov). As Aca2 levels rise, it binds to the operon’s promoter and shuts off further transcription of both genes – establishing a negative feedback loop (autoregulation) (pmc.ncbi.nlm.nih.gov). This timing ensures a window of AcrIF8 production sufficient for phage DNA protection, followed by repression to prevent overshoot. The promoter region contains two inverted repeat (IR) operator sites, termed IR1 and IR2, which mediate Aca2 binding (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). IR1 overlaps the core promoter (−35 and −10 elements) and has high affinity for Aca2, making it the primary operator that, when occupied, physically blocks RNA polymerase binding and transcription initiation (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). IR2 is a secondary site of lower affinity, located nearby – it does not significantly contribute to repression once lysogeny is established, but it can bind Aca2 at higher concentrations, likely playing a role during the acute infection phase when Aca2 is just beginning to accumulate (pmc.ncbi.nlm.nih.gov). This two-site arrangement is thought to fine-tune the repression: IR1 ensures strong repression even at moderate Aca2 levels, while IR2 provides an additional check only when Aca2 is abundant, perhaps preventing any leaky transcription under high phage copy conditions (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). The slight differences in sequence and Aca2 affinity between IR1 and IR2 have likely evolved to modulate anti-CRISPR output at different stages of infection (pmc.ncbi.nlm.nih.gov). Collectively, these features create a tightly regulated switch: high acrIF8–aca2 expression early on, then shutoff via Aca2 binding as the system transitions to lysogeny or a maintenance phase (pmc.ncbi.nlm.nih.gov).
Induction and Environmental Regulation: Under normal lysogenic conditions (when ZF40 is integrated in the bacterial genome), the acrIF8–aca2 operon is kept repressed by Aca2, resulting in very low baseline expression of both AcrIF8 and Aca2. This likely limits any fitness burden on the host cell during lysogeny. If the prophage is induced into the lytic cycle (for example by stress triggers that also induce the SOS response), it is conceivable that repression by Aca2 must be relieved to re-enable anti-CRISPR expression for that lytic episode. The precise mechanism for lifting Aca2 repression during prophage induction is not yet fully elucidated. It could involve Aca2 dilution or inactivation (some phage repressors are inactivated by host proteases or SOS-induced cleavage, though Aca2’s susceptibility to such mechanisms is unconfirmed). Experimental data suggest that an additional factor or condition might be required to completely reactivate the operon in vivo, as in vitro DNA-binding assays showed Aca2 binding alone is very strong (pmc.ncbi.nlm.nih.gov). It is possible that host or phage-encoded signals modulate Aca2’s binding under specific circumstances, but further research is needed. Nonetheless, upon new infection of a cell, Aca2 repression will not exist initially (since no Aca2 protein is present in the incoming virion), which allows a fresh round of acrIF8–aca2 expression to occur unimpeded. Summarily, expression of Aca2 is tightly coupled to phage infection cycles: it is off (repressed) during quiescent lysogeny, sharply on in early infection, and then self-terminates. This pattern is optimal for a temperate phage’s need to balance aggressive offense (immunity evasion via Acr) with long-term coexistence (lysogen survival via repression of Acr). The regulation is principally at the transcriptional level via the promoter operators, complemented by Aca2’s post-transcriptional mRNA binding which provides a fast-acting layer of control as transcripts accumulate (www.nature.com). In GO annotation terms, Aca2 is involved in autoregulation of transcription and feedback control of gene expression.
Aca Protein Family: Aca2 belongs to a broader family of Anti-CRISPR associated (Aca) proteins, which are found in many bacteriophages and other mobile genetic elements. At least eight distinct Aca families (Aca1–Aca8) have been identified so far, each defined by sequence homology and typically linked to particular types of anti-CRISPR genes (pmc.ncbi.nlm.nih.gov). All Aca proteins are small HTH-domain regulators, but across families they share low sequence identity and recognize different DNA motifs in their target promoters (pmc.ncbi.nlm.nih.gov). Aca2 represents one such family; its homologs (Aca2-like proteins) have been detected in phage genomes infecting diverse bacterial hosts. Bioinformatic surveys using hidden Markov models found aca2-like genes widely distributed in bacteria, including in genomes that do not yet have characterized acr genes (pmc.ncbi.nlm.nih.gov). This suggests Aca2 homologs are pervasive and may sometimes regulate genes other than anti-CRISPRs. Members of the Aca2 family are typically around 110–120 amino acids (consistent with ZF40 Aca2’s 116 aa) and all possess the hallmark extended C-terminus for dimerization not seen in the shorter Aca1 family (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). Key functional residues (in the HTH and dimer interface) are conserved among Aca2 homologs, indicating strong evolutionary pressure to maintain the mode of DNA binding and repression (pmc.ncbi.nlm.nih.gov). The mechanism of Acr operon repression by Aca proteins appears to be conserved broadly: for each known Aca family, researchers have identified a cognate inverted repeat sequence in the acr–aca operon promoter, and demonstrated that the corresponding Aca protein can repress transcription from that promoter (pmc.ncbi.nlm.nih.gov). A recent comparative study confirmed that acr repression by Aca proteins is widespread in nature, with Aca proteins acting as auto-repressors in many phage/host systems (pmc.ncbi.nlm.nih.gov).
Homologous and Analogous Proteins: Beyond the anti-CRISPR context, Aca2 is part of the large superclass of prokaryotic HTH transcriptional regulators. Its nearest functional analogs are phage or plasmid-encoded repressors that regulate gene modules for host interaction. For example, Pseudomonas phages often carry an Aca1 protein, which, like Aca2, represses its acr–aca1 operon (in that case often targeting type I-F or I-E CRISPR systems) (pmc.ncbi.nlm.nih.gov). While Aca1 and Aca2 differ in size and sequence, their overall roles (anti-CRISPR operon autoregulation) are analogous, and structural studies show they both utilize an HTH for DNA binding but dimerize differently (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). Outside of phages, the similarity to the bacterial antitoxin MqsA (noted above) suggests a possible distant relationship or convergent evolution between anti-CRISPR repressors and toxin–antitoxin system regulators (pmc.ncbi.nlm.nih.gov). This is plausible as both serve as stress-response transcriptional regulators. However, Aca2’s dual DNA/RNA binding capability noted in phage ZF40 might be a more specialized adaptation; it is currently unknown in many other systems but appears to be a feature conserved at least within the Aca2 family of proteins (www.rcsb.org). Indeed, the RNA-binding function was found to be shared among several Aca2 homologs, implying that dual control (transcriptional and translational repression) could be an evolutionary strategy in this family to cope with rapidly replicating genomes and transcript surges (www.rcsb.org). In summary, Aca2 is conserved as a functional type across many phages: wherever an acr gene needs regulation, an Aca repressor of some family is often present. The Aca2-type regulators specifically are one such lineage, conserved in sequence features and regulatory roles in diverse microbial genetic elements, highlighting a successful evolutionary tactic for managing anti-immunity genes.
2019 (Nucleic Acids Research – Birkholz et al.): The Aca2 protein was functionally characterized as an autorepressor of the acrIF8-aca2 operon in phage ZF40 (pmc.ncbi.nlm.nih.gov). Birkholz and colleagues demonstrated that Aca2 forms dimers and binds two inverted repeat sequences in the operon’s promoter to repress its transcription (pmc.ncbi.nlm.nih.gov). DNA footprinting and mutational analyses showed that binding at these sites (especially IR1) is required to shut off acrIF8 expression. This study provided the first direct evidence that anti-CRISPR associated genes (aca) indeed encode transcriptional repressors for acr genes (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). It also introduced Aca2 as a model for understanding the “anti-anti-CRISPR” regulatory loop in phages.
2021 (J. Structural Biology – Usher et al. & J. Biol. Chem. – Liu et al.): Two independent groups solved the crystal structure of Aca2 and elucidated its mechanism at the molecular level. Usher et al. resolved the apo-Aca2 dimer structure at 1.34 Å, revealing the HTH motif and the extended dimerization interface unique to Aca2 (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). They confirmed that Aca2’s operator overlaps the –35/–10 promoter elements, explaining repression by steric hindrance of RNA polymerase (pmc.ncbi.nlm.nih.gov). Liu et al. determined structures of Aca2 (from ZF40) both alone and bound to its IR1 operator DNA (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). Their study showed that each Aca2 dimer binds one IR1 site without bending the DNA significantly, in contrast to Aca1 which induced DNA bending (pmc.ncbi.nlm.nih.gov). Key residues for DNA recognition (in helix α3) and for dimerization were identified and validated by mutagenesis and reporter assays (pmc.ncbi.nlm.nih.gov) (pmc.ncbi.nlm.nih.gov). These works collectively provided a structural basis for Aca2 function, confirming its two-domain architecture (DNA-binding NTD and dimerization CTD) and the conserved mode of binding to operator DNA as a homodimer.
2022 (Nucleic Acids Research – Fagerlund et al.): Researchers performed a comprehensive bioinformatic and experimental survey of Aca proteins across bacteria (pmc.ncbi.nlm.nih.gov). They found that Aca-mediated repression is widespread: using consensus sequence models for each Aca family (Aca1–Aca8), they identified putative acr-aca operons in numerous genomes and showed in E. coli reporter systems that these promoters are repressed by their cognate Aca proteins (pmc.ncbi.nlm.nih.gov). This study underscored the generality of the mechanism first shown with Aca2 – i.e., Acr gene production is commonly kept in check by a neighboring HTH repressor – highlighting that Aca2 is one example of a broader paradigm in phage biology.
2024 (Nature – Birkholz et al.): New research uncovered a dual role of Aca2 in controlling anti-CRISPR levels (www.nature.com). Birkholz and co-workers discovered that Aca2 not only represses transcription of acrIF8, but also binds to the acrIF8–aca2 mRNA to inhibit its translation (www.nature.com). They solved a cryo-EM structure of Aca2 bound to an RNA stem-loop, revealing how the protein’s HTH domain can switch between DNA and RNA targets (www.nature.com). Functional assays indicated that this combined transcriptional and translational repression is crucial for managing acr expression when phage DNA is replicating rapidly (www.rcsb.org). This advanced our understanding by showing Aca2 as a multimodal regulator, and provided a rare example of an HTH protein that moonlights in RNA binding. The findings also demonstrated that Aca2’s dual mechanism is conserved among its homologs, emphasizing its evolutionary innovation (www.rcsb.org).
2024 (J. Biol. Chem. – phage engineering study): Fineran and colleagues applied endogenous CRISPR-Cas selection to engineer phage ZF40 and directly test Aca2’s importance (www.jbc.org) (www.jbc.org). They reported that deleting aca2 is lethal to the phage, as Aca2-null phages could not form plaques (no viable lytic growth) (www.jbc.org). They further showed that without Aca2, the acrIF8-aca2 promoter becomes constitutively active, leading to excessive AcrIF8 levels that hinder phage replication and even harm the host cell (www.jbc.org). Conversely, when acrIF8 was overexpressed from a plasmid, it reduced bacterial conjugation efficiency, confirming AcrIF8’s toxicity at high dosage (www.jbc.org). These experiments provided genetic proof of Aca2’s essential role in the phage lifecycle and illustrated the delicate balance Aca2 mediates between phage and host viability.
Each of these studies contributes to a comprehensive picture of Aca2: from initial discovery of its function, through structural and mechanistic insight, to the latest understanding of its dual activity and vital importance for phage success. Together, they establish Aca2 as a critical gene for GO annotation in areas of transcriptional regulation, virus-host interaction, and immune evasion.
Based on the above information, the following Gene Ontology terms are applicable to Aca2:
Identical protein binding – Aca2 forms homodimers, interacting with itself to become functional (pmc.ncbi.nlm.nih.gov).
Biological Process (BP):
DNA integration into host DNA (lysogeny) – By enabling stable maintenance of the prophage (through controlled Acr expression), Aca2 is associated with successful viral genome integration and latency (pmc.ncbi.nlm.nih.gov).
Cellular Component (CC):
Each of these GO terms can be supported by the experimental evidence cited above, helping to annotate Aca2’s role as a DNA/RNA-binding transcriptional repressor involved in phage immune evasion and life cycle regulation. The combination of molecular functions and biological processes reflects Aca2’s unique dual regulatory activity and its importance in the virus-bacteria interaction context.
References: The information above is supported by key studies and reviews on Aca2 and anti-CRISPR systems (pmc.ncbi.nlm.nih.gov) (www.nature.com) (pmc.ncbi.nlm.nih.gov) (www.rcsb.org), as cited throughout the report. This ensures that each asserted function, process, and feature of the Aca2 protein is backed by experimental evidence, providing a solid basis for Gene Ontology annotation curation.