Poly(A) binding protein

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Poly(A) binding protein

Structure

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1 Introduction
2 Function
- 2.1 Poly (A)Binding
  - 2.1.1 Adenosine Stabilization Interaction Patterns
- 2.2 Translation Initiation
  - 2.2.1 Structural Components of PABP Translation Initiation
3 Medical Relevancy
- 3.1 Rotavirus' Effect on Initiation of Translation
4 Biological Relevancy
- 4.1 Poly(A) Binding Protein's Evolution in plants
5 References

Introduction

Figure 1: PABP Biological Assembly with linker highlighted.

Human Poly(A) Binding Protein (PABP) is a biopolypeptide involved in recognizing the 3' poly(A) tail of mRNA that is added to an mRNA transcript during mRNA processing.This recognition as well as PABP's interaction with other proteins and initiation factors causes it to also play a significant role in translation initiation and mRNA stabilization and degradation. PABP consists of four conserved domains of RNA recognition motifs (RRMs); however, the two N-terminal RRMs (RRM1 and RRM2) and the short linker sequence that connects them supports most of the function of PABP, so RRM3 and RRM4 may not be essential. Thus, the published X-ray structure, found by X-ray diffraction, exhibits RRM1 and RRM2 at a 2.6 Angstrom resolution. This is shown as . Both RRM 1 and 2 are needed to support biochemical function, that is, no one RRM can support biochemical function. Additionally, there is a proline rich C-terminal portion of variable length that is not well conserved and unknown as to how it contributes to the protein's function ^[3].

Function

Poly (A)Binding

Figure 2: The specific weak intermolecular interactions between RNP1 and RNP2 and Adenosines. These interactions are the primary support of adenosine recognition by PABP and include mainly van der Waals interactions, hydrogen bonds, and stacking interactions.

A primary function of PABP is recognizing and interacting with the 3'poly (A) tail created in mRNA processing. As found by EMSA competition experiments, there is a minimum of 11-12 adenosines necessary in the poly (A) tail for the adenosine chain to bind to PABP with high affinity. However, for one biological assembly, a chain containing 9 adenosines sufficiently binds the assembly for crystallization and is shown in the biological assembly structure. The 4 RRM domains that are the primary interacting sites for the adenosine recognition exist as globular domains, each having four antiparallel β-strands and two α-helices. With the N-terminal to C-terminal motifs labeled as S1 to S4 for the β-strands and H1 to H2 for the α-helices, the strands are spatially arranged as S2-S3-S1-S4. Furthermore, there are two conserved sequences in each RRM, called RNP1 and 2. RNP 1 consists of a conserved sequence of 8 residues, while RNP2 consists of a conserved sequence of 6 residues. Much of the weak intermolecular interactions with adenosine from the RRMs occur from the conserved sequences, which correspond to the two central β-strands, with specific interactions shown in Figure 2.The support for adenosine recognition by the RRMs occurs as a type of binding trough with the sheets, primarily , and the interstrand loop between β-strands 2 and 3 as well as the domain linker forming the . It is believed that the is disordered in the absence of RNA because it does not intramolecularly interact with either of the RRM motifs. Additionally, the primary binding trough is stabilized by . ^[3]

Figure 3: Basic residues of RRM 1 and 2 (shown in blue) make stabilizing electrostatic interactions with the negatively charged adenosine phosphates.

Adenosine Stabilization Interaction Patterns

Specifically, there are several significant interaction patterns that stabilize adenosine recognition. RRM 1 and 2 makes significant interactions with the adenosine backbone, shown in Figure 3. Additionally, the adenosine stabilizes itself within the binding by intramolecular stacking interactions between adenosines. Through the extensive , the RRM specifies the position of adenosine 2, allowing it to make strong intramolecular stacking interactions with adenosine 1. As a result, adenosine 1 requires less contact with the RRM, as it is mostly stabilized by adenosine 2. Furthermore, some adenosines like adenosine 3 and adenosine 6 are stabilized by being sandwiched between aromatic and alipathic side chains. occurs between aromatic and alipathic side chains and is specified by Lysine 104, and occurs similarly, but it is specified doubly by two residues, Trp-86 and Gln-88 ^[3].

Translation Initiation

Figure 4:Closed loop model diagram required for translation initiation in eukaryotes.

The initiation of translation in eukaryotes requires many translation factors and proteins, one of which is PABP. There is evidence that PABP is critical for formation of the “closed loop” model of protein synthesis, which involves joining the 3’ poly (A) tail of mRNA to the 5’ cap to create circular RNA ^[4]. This process utilizes eIF4F, a protein composed of multiple translation factors that play various roles in translation. eIF4G is a scaffolding protein that binds the other subunits, eIF4E and eIF4A. eIF4E creates interactions with the 5’ cap to bring the initiation factor (IF) complex to the 5’ end of the mRNA. eIF4A is an RNA helicase that denatures RNA and allows the ribosome to move along the strand. eIF4G also has a binding site for PABP, which is N-terminal to the binding site for eIF4F and interacts with the same RRMs that allow PABP to bind RNA. ^[5] All of these proteins are known to be involved in protein synthesis, but several mechanisms have been proposed for how PABP might be promoting translation.

By observing protein synthesis in cells deficient of PABP, Kahvejian et al. were able to show that the PABP/eIF4G interaction promotes translation. The cells lacking PABP showed a seven-fold decrease in the rate of translation, which was remedied by reintroducing PABP to the cells. Other cells were treated with a PABP mutant that also had an eIF4G binding site, but the introduction of these proteins did not return the rate of translation to its normal level ^[6]. These results show that not only is PABP acting as a translation factor in eukaryotic cells, but it also needs to interact with eIF4G in order to have an effect.

Furthermore, PABP interactions have been shown to be critical for the binding of the 80S ribosomal subunit. In a similar experiment, cells that were deficient in PABP were observed for binding of the 80S subunit, and researchers saw a binding reduction of greater than 60%. Reintroducing PABP to these cells restored ribosomal binding and even promoted the formation of the 80S initiation complex. These results display the importance of PABP in recruiting the 80S ribosomal subunit for the initiation of translation. A similar experiment was run In order to determine whether decreased 80S ribosomal recruitment was due to a decrease in 40S ribosomal recruitment. Results showed that PABP is also involved in recruiting the 40S ribosomal subunit to the RNA ^[6]. Because of this, PABP affects the binding of the 80S subunit in two ways: indirectly, by allowing the 40S subunit to be available to bind, and directly, by promoting association of the 80S subunit with the 40S subunit.

In addition to these interactions, the PABP aids in this closed loop formation via interactions with Poly (A) Interacting Protein 1 (PAIP-1). In this process, PABP interacts with PAIP-1 to facilitate the complex to interact with eIF4A initiation factor. eIF4A unwinds the 5' untranslated region (UTR) of an mRNA transcript, which signals eIF4G to function as previously mentioned ^[3]. Thus, there are two mechanisms to initiate this loop closing pathway with eIF4G. All of these proposed interactions show that PABP stimulates translation at several points throughout the initiation process.

Structural Components of PABP Translation Initiation

The RRMs support interactions with the interacting proteins such as eIF4G and PAIP-1, however, the specific ways in which PABP interacts with these proteins are not structurally proven. However, there is a convex dorsal surface present on the RRM 1 and 2 motifs formed by the two α-helices in each RRM, specified as H1 and H2 in RRM1 and H1' and H2' in RRM2. This surface contains a sequence portion of and residues. It is thought that this area of conservation thus produces overlapping binding sites to interact with eIF4G and PAIP-1. For example, the conserved acidic residues may be beneficial to be used in to interact with essential basic residues present in both eIF4G and PAIP-1 via ionic interactions ^[3].

Medical Relevancy

Rotavirus' Effect on Initiation of Translation

The initiation of translation in eukaryotes is supported by a closed loop model. This model requires the 5' end and the 3' end of mRNA to be physically connected. The poly(A)-binding protein is necessary for initiation of translation and is required for the closed loop model. Rotavirus, a virus of varying size, containing 11 double stranded RNA and 12 proteins (6 structural, 6 non-structural) is responsible for preventing initiation of translation in infected cells. The virus enters the cell and undergoes a non-conservative replication cycle in the cytoplasm. After a replication cycle non-structural protein 3 (NSP3) can be found spread throughout the cytoplasm. NSP3 is responsible for releasing PABP from eIF4F and inhibiting translation initiation. In a study done by Piron et al. it has been seen that NSP3 competes with PABP in binding to the poly(A)-tail of mRNA. This competitor inhibits the proper closing of the closed loop therefore inhibiting translation and protein synthesis. Not only does the rotavirus inhibit protein synthesis of the host cell but it successfully initiatives its own translation as well. The viral mRNA and the host translation initiation factors are in close enough proximity to allow the viral mRNA bound to NSP3 to undergo translation. The translation of viral mRNA allows the virus to spread throughout an organism and lead to a greater decrease in host protein synthesis. When infected with rotavirus one may experience diarrhea, fever, vomiting, and dehydration. Without an antiviral it is suggested to increase fluid intake and allow three to seven days for the infection to subside. ^[7]

Biological Relevancy