A-type Particles Research Articles

Early time wetting kinetics in surface-directed spinodal decomposition for off-critical quenches: A molecular dynamics study.

We present results from the molecular dynamics simulation of surface-directed spinodal decomposition in binary fluid mixtures (A + B) with off-critical compositions. The aim is to elucidate the role of composition ratio in the early time wetting kinetics under the influence of long-range surface potential. In our simulations, the attractive part of surface potential varies as V(z) = -ϵa/zn, with ϵa being the surface-potential strength. The surface prefers the "A" species to form the wetting layer. Its thickness [R1(t)] for the majority wetting (number of A-type particles [NA] > number of B-type particles [NB]) grows as a power-law with an exponent of 1/(n + 2). This is consistent with the early time kinetics in the form of potential-dependent growth present in the Puri-Binder model. However, for minority wetting (NA < NB), the growth exponent in R1(t) is less than 1/(n + 2). Furthermore, on decreasing the field strength ϵa, we recover 1/(n + 2) for a minority wetting case. We provide phenomenological arguments to explain the early time wetting kinetics for both cases.

Effect of Copper Antifouling Paint on Marine Degradation of Polypropylene: Uneven Distribution of Microdebris between Nagasaki Port and Goto Island, Japan.

Microplastics (MP) encompass not only plastic products but also paint particles. Marine microdebris, including MP, was retrieved from five sampling stations spanning Nagasaki-Goto island and was classified into six types, primarily consisting of MP (A), Si-based (B), and Cu-based (C) paint particles. Type-A particles, i.e., MP, were exceedingly small, with 74% of them having a long diameter of 25 µm or less. The vertical distribution of type C, containing cuprous oxide, exhibited no depth dependence, with its dominant size being less than 7 μm. It was considered that the presence of type C was associated with a natural phenomenon of MP loss. To clarify this, polypropylene (PP) samples containing cuprous oxide were prepared, and their accelerated degradation behavior was studied using a novel enhanced degradation method employing a sulfate ion radical as an initiator. Infrared spectroscopy revealed the formation of a copper soap compound in seawater. Scanning electron microscopy/energy-dispersive X-ray spectroscopy analysis indicated that the chemical reactions between Cl- and cuprous oxide produced Cu+ ions. The acceleration of degradation induced by the copper soap formed was studied through the changes in the number of PP chain scissions, revealing that the presence of type-C accelerated MP degradation.

Vibro-fluidization of cohesive particles

The paper assesses the behavior of cohesive Geldart C-type particles, when fluidized by air with the aid of vibration. Together with their poor flowability and irregular hopper discharge, bubbling fluidization is very difficult to achieve due to the possible particle agglomeration and gas channeling. When trying to fluidize cohesive particles, the gas drag force cannot break the inter-particle bonds. Despite all these handling and operation problems, ultrafine particles of micron- or nanosize are increasingly applied in industrial processes. To disrupt the stable gas channels and cracks, a mechanical vibration is one of the easier and preferred methods to improve the fluidity of the cohesive particles. In the present study, several 2 to 40 μm particles were used. A comparison with Geldart A-type particles was also made. Experimental results were used to validate a more fundamental approach based upon the balance of forces acting on the particles. This resulted in a new delineation of the Geldart C/A boundary where the critical transition particle size for particles of given absolute density, ρp, Hamaker constant, H, and inter-particle distance, z0, decreases with an increasing vibration intensity, I, according to dcrit2ρp=8.03Hz021+Ig.

Mechanisms of like-charge attraction in many-body systems

The physics of like-charge attraction in a collinear binary system of N particles has been investigated via a polarizable-ion model. It was found that like-charge attraction between an array of (N−1) type-A particles on the left and a single type-B particle on the right is conditional upon a sufficient degree of dissimilarities between the two types of particles. By assuming that (1) the particles of one type are strongly polarizing (but weakly polarizable) such that the Coulomb fields they produce are dominant all over other electric fields, and that (2) the particles of the other type are strongly polarizable (but weakly polarizing) such that their Coulomb-field-induced dipoles are the only polarization effects worth considering, a good agreement between our approximate analytic theory and exact numerical solutions has been obtained. Our analytic results show that the attractive components of the electrostatic force between the two types of particles could be thought of as arising from imaginary charges induced in the polarized particle(s) by the polarizing ones, resulting in a screening of the real charge(s) in the polarized particle(s). Like-charge attraction occurs if the field contributions from the imaginary charges collectively outweigh the field contribution(s) from the real charge(s).

POGZ suppresses 2C transcriptional program and retrotransposable elements

The POGZ gene has been found frequently mutated in neurodevelopmental disorders (NDDs) such as autism spectrum disorder (ASD) and intellectual disability (ID). We have recently shown that POGZ maintains mouse embryonic stem cells (ESCs). However, the exact mechanisms remain unclear. Here, we show that POGZ plays an important role in the maintenance of ESCs by silencing Dux and endogenous retroviruses (ERVs). POGZ maintains a silent chromatin state at Dux and ERVs by associating with and recruiting TRIM28 and SETDB1, and its loss leads to decreased levels of H3K9me3/H4K20me3, resulting in up-regulation of 2C transcripts and ESC transition to a 2C-like state. POGZ suppresses different classes of ERVs through direct (IAPEy, the intracisternal A-type particle elements) and indirect regulation (MERVL). Activation of POGZ-bound ERVs is associated with up-regulation of nearby neural disease genes such as Serpina3m. Our findings provide important insights into understanding the disease mechanism caused by POGZ dysfunction.

Co-option of endogenous retroviruses through genetic escape from TRIM28 repression

Endogenous retroviruses (ERVs) have rewired host gene networks. To explore the origins of co-option, we employed an active murine ERV, IAPEz, and an embryonic stem cell (ESC) to neural progenitor cell (NPC) differentiation model. Transcriptional silencing via TRIM28 maps to a 190bp sequence encoding the intracisternal A-type particle (IAP) signal peptide, which confers retrotransposition activity. A subset of "escapee" IAPs (∼15%) exhibits significant genetic divergence from this sequence. Canonical repressed IAPs succumb to a previously undocumented demarcation by H3K9me3 and H3K27me3 in NPCs. Escapee IAPs, in contrast, evade repression in both cell types, resulting in their transcriptional derepression, particularly in NPCs. We validate the enhancer function of a 47bp sequence within the U3 region of the long terminal repeat (LTR) and show that escapee IAPs convey an activating effect on nearby neural genes. In sum, co-opted ERVs stem from genetic escapees that have lost vital sequences required for both TRIM28 restriction and autonomous retrotransposition.

Impact of solvent polarity on the morphology, physicochemical properties, and digestibility of A-type resistant starch particles

Resistant starch particles (RSP) formed by antisolvent precipitation method has attracted much attention as a functional food ingredient having beneficial effects on obesity and diabetes. However, the effect of solvent polarity on the physicochemical properties and digestibility of RSP remains unclear. Here, n-propanol, isopropanol, acetone, and ethanol were employed as antisolvents to prepare RSP. The width and length of the resulting RSP decreased from 0.87 μm to 0.59 μm and from 2.56 μm to 1.31 μm, respectively, upon increasing the solvent polarity, while dramatically decreasing their crystallinity and the gelatinization enthalpy from 80.5% to 62.3% and from 67.9 ± 14.4 J/g to 41.5 ± 8.3 J/g, respectively, suggesting that solvent polarity is critical factor determining morphology, crystallinity, and thermostability of RSP. Furthermore, the level of resistant starch in RSP was found to be inversely proportional to the degree of solvent polarity, which would provide a useful means for modulating the digestibility of RSP.

Selection of Relative DEM Time Step for Modelling Fast Fluidized Bed of A-Type FCC Particles

In chemical production processes, the most suitable operation regime for A-Type powders such as typical FCC particles is high-speed fast fluidization owing to their uniquely advantageous properties. Discrete element method (DEM) for modelling fast fluidization with A-Type powders has rarely been reported. How to appropriately select the DEM time step and the stiffness coefficient is one of the most critical problems for stable and accurate calculation. This article mainly discusses the effect of the stiffness coefficient and DEM time step on simulations of A-type FCC particles. In order to describe the effect of both parameters and their complex interaction, a dimensionless relative DEM time step is introduced. In total, nine cases with different numbers of relative time steps are adopted for modelling a microfluidized bed of A-Type FCC particles, the regime of which is proved to be fast fluidization. Results show that three bifurcations occur in all the simulations. Only the moderate relative time step possesses the capability of modelling the process of particle collision and thus predicts the right flow regime with asymmetric and heterogeneous typical fast fluidized structures. When the relative time step increases to large rank, simulations predict untrue fluidization regimes with symmetric and homogeneous structures. Moreover, both over-large and over-low relative time steps cause excessive particle overlap and thus a divergence of simulation. The further optimization of moderate relative DEM time step in relation to real particle property is unidentifiable and is thus an outstanding issue. That the range of the moderate relative time step is limited indicates that the common soft-sphere model is poor at modelling fast fluidization of A-Type particles. It is suggested that possible future work should be focused on improving the simulation frame and employing the molecular dynamics model to more appropriately deal with particle contact.

Mechanisms of like-charge attraction in three-body systems

The physics of like-charge attraction in three-body systems has been investigated via a polarizable-ion model. It was found that like-charge attraction is possible for two configurations of a collinear binary system with regular interparticle spacings. For the mirror-symmetric configuration ABA, the dominant mechanism of like-charge attraction between the type-B particle and each type-A particle is the polarization of each type-A particle by the type-B particle. For the mirror-asymmetric configuration AAB, the dominant mechanism of like-charge attraction between the type-B particle and the pair of type-A particles is either the polarization of the pair of type-A particles by the type-B particle, or vice versa. For either configuration, the occurrence of like-charge attraction is conditional upon the presence of dissimilarities in net charge or polarizable volume between the two types of particles, as in the case of a two-particle system. The findings point to a new direction for manipulating interactions of polarizable particles at the micro- or nano-scale.

Targeted Synthesis of the Type-A Particle Substructure from Enzymatically Produced Eumelanin.

Eumelanin exhibits a defined supramolecular buildup that is deprived of at least three distinct particle species. To enable the full potential of its promising material properties, access to all particle types is crucial. In this work, the first protocol for the synthesis of the intermediate type-A particles in pure and stable dispersion form is described. It is found that aggregation of type-A particles into the larger type-B variant can be inhibited by a strict pH control during the synthesis. The exact influence of pH on the supramolecular buildup is investigated via a combination of time-resolved light scattering, electron microscopy, and UV–vis spectroscopy. It is observed that a rapid buildup of type-B particles occurs without pH control and is generally dominant at lower pH values. At pH values above 6.2 however, type-A particles are gained, and no further aggregation occurs. Even more, lowering the pH of such a stable type-A dispersion at a later stage lifts the inhibition and again leads to the formation of larger particle species. The results confirm that it is easily possible to halt the aggregation of eumelanin substructures and to access them in the form of a stable dispersion. Moreover, a profound additional understanding of the supramolecular buildup is gained by the in-depth investigation of the pH influence.

Real-time measurements of fluorescent aerosol particles in a living laboratory office under variable human occupancy and ventilation conditions

The abundance of super-micron biological and abiotic particles in occupied indoor environments can be influenced by time-dependent changes in human-associated emissions and building ventilation conditions. Real-time measurements of fluorescent aerosol particles (FAPs) were integrated with a building sensing platform to evaluate the influence of human occupancy and ventilation on the temporal dynamics of fluorescent biological and abiotic particles in a living laboratory office. Concentrations and size distributions of FAPs were measured via laser-induced fluorescence (LIF). Human occupants were identified as a major source of super-micron FAPs in mechanically ventilated office buildings. Mass concentrations and size distributions of FAPs larger than 3 μm scaled with human occupancy in the office. Detailed single particle fluorescence data indicated that human-associated emissions enriched the office atmosphere with specific FAP types that varied in morphology. Office occupants were strong emitters of ABC-type particles (number and mass), and to a lesser extent, A-type particles (number and mass), AB-type particles (mass), and B-type particles (mass). Such FAP types are related to common indoor bacterial and fungal aerosols and fluorescent clothing fabric fibers. The introduction of natural ventilation via a double skin glass façade increased the indoor abundance of FAPs due to the efficient transport of outdoor FAPs into the office. While LIF provides valuable real-time data on indoor FAP dynamics, it lacks specificity and cannot fully resolve the origins of fluorescent biological and abiotic particles in indoor spaces.

Thermal energy storage in fluidized bed using microencapsulated phase change materials

Fluidized beds are widely used in effective heat and mass transfer applications for chemical processes. The beds can also used for storing thermal energy (TES) and offer a rapid and effective way to exploit solar energy especially for heating applications. Microencapsulated PCMs serve as the TES medium and the fluid phase in these applications. There exist few experimental studies that have investigated uses of fluidized beds for thermal storage. The works show that properties of microencapsulated PCMs have to be fine-tuned for them to become effective in fluidized beds. This paper investigates the performance of an experimental air-fluidized bed using microencapsulated PCM as the thermal storage system for two different storage temperatures of 55 °C and 65 °C. The results show that TES using microencapsulated PCM with mean particle size of 100 μm that corresponds to A-type particle according to Geldart chart showing fluidization behavior of particles is possible. The fluidization process did not change the morphology of the microencapsulated PCM. Fast storage and recovery can easily be accomplished at efficiencies as high as 80%.

Characterization of two types of cesium-bearing microparticles emitted from the Fukushima accident via multiple synchrotron radiation analyses

A part of radiocesium emitted during the Fukushima nuclear accident was incorporated in glassy water-resistant microparticles, called Type-A particles, which are spherical with ~ 0.1 to 10 µm diameter and ~ 10–2 to 102 Bq cesium-137 (137Cs) radioactivity; they were emitted from Unit 2 or 3 of the Fukushima Daiichi Nuclear Power Plant. Meanwhile, Type-B particles, having various shapes, 50–400 µm diameter, and 101–104 Bq 137Cs radioactivity, were emitted from Unit 1. The chemical properties of these radioactive particles have been reported in detail, but previous studies investigated only a small number of particles, especially Type-B particles. We tried to understand radioactive particles systematically by analyzing a large number of particles. Micro-X-ray computed tomography combined with X-ray fluorescence analysis revealed the presence of many voids and iron-rich part within Type-B particles. The 137Cs concentration (Bq mm–3) of Type-A particles was ~ 10,000 times higher than that of Type-B particles. Among the Type-B particles, the spherical ones had higher concentration of volatile elements than the non-spherical ones. These differences suggested that Type-A particles were formed through gas condensation, whereas Type-B particles were formed through melt solidification. These findings might contribute to the safe decommissioning of reactors and environmental impact assessment.

SMARCAD1 ATPase activity is required to silence endogenous retroviruses in embryonic stem cells

Endogenous retroviruses (ERVs) can confer benefits to their host but present a threat to genome integrity if not regulated correctly. Here we identify the SWI/SNF-like remodeler SMARCAD1 as a key factor in the control of ERVs in embryonic stem cells. SMARCAD1 is enriched at ERV subfamilies class I and II, particularly at active intracisternal A-type particles (IAPs), where it preserves repressive histone methylation marks. Depletion of SMARCAD1 results in de-repression of IAPs and adjacent genes. Recruitment of SMARCAD1 to ERVs is dependent on KAP1, a central component of the silencing machinery. SMARCAD1 and KAP1 occupancy at ERVs is co-dependent and requires the ATPase function of SMARCAD1. Our findings uncover a role for the enzymatic activity of SMARCAD1 in cooperating with KAP1 to silence ERVs. This reveals ATP-dependent chromatin remodeling as an integral step in retrotransposon regulation in stem cells and advances our understanding of the mechanisms driving heterochromatin establishment.

Mesoscale Simulation of self-diffusiophoretic microrotor

Artificial micro-scale or nano-scale machines that are capable of converting energy to mechanical work, have long been pursued by science and engineering communities for their potential applications in microfluidics, biology and medicine. From a physics point of view, they are also ideal models to investigate fundamental statistical phenomena in non-equilibrium active matters. Inspired by bio-machines and bio-motors like ATP synthase and flagellum motors, we propose a simple design of rotary motors based on pure self-diffusiophoresis effects. The basic design of the rotor consists of three colloidal beads with different surface properties, which leads to different interactions between the beads and solvent molecules. Chemical reactions are imposed on the surface of one of the beads, which creates a source of one of the two solvent molecules and generates a local concentration gradient. The other two beads connected to the catalytic bead have different affinities to the solvent molecules, which leads to asymmetric diffusiophoretic forces on the two non-catalytic beads. A net torque is thus obtained from difference of the diffusiophoretic forces between the two non-catalytic beads. In our simulation, we employ hybrid molecular dynamics (MD) simulations and multi-particle collision dynamics (MPC) to investigate the motion of microrotors. The binary fluid is composed with A-type and B-type solvent particle whose interactions are described by multi-particle collision dynamics while beads-particle interactions are modeled by molecular dynamics. In MPC, all fluid particles execute alternating streaming and collision steps. During streaming steps, the solvents move ballistically. During collision steps, particles are sorted into square cells and only interact with particles in the same cell under a specific stochastic rotation rule. MPC algorithm locally conserves mass, linear momentum, angular momentum and energy, and properly captures thermal fluctuation, mass diffusion, dissipation and hydrodynamic interactions. In our simulation, standard MPC parameters are employed which correspond to a liquid-like behavior of fluid. In MD, beads-solvent interactions are described by Lennard-Jones(LJ) potential with different parameter combinations and the equations of motion is integrated by velocity-Verlet algorithm. To perform hybrid molecular dynamic simulations with multi-particle collision dynamics, between two MPC collision steps, 50 MD steps are implemented for the solvent particles that are in the interaction range of colloidal beads. We first investigate the solvent concentration distribution around static microrotor, and confirm that the catalytic bead generates a steady-state local concentration gradient. Net angular displacements are obtained when the rotor is allowed to rotate freely. The rotational direction and speed of the micorotor are determined by bead-solvent interactions, the rotor geometry, the solvent viscosity and the catalytic reaction ratio. We also study the scenario in which two rotors are placed in close vicinity to each other. We find that the coupling between the concentration fields around the rotors reduces the rotational speed of both rotors.

Histone H3.3 is required for endogenous retroviral element silencing in embryonic stem cells.

Transposable elements (TEs) comprise roughly forty per cent of mammalian genomes1. TEs have played an active role in genetic variation, adaptation, and evolution through the duplication or deletion of genes or their regulatory elements2-4 and TEs themselves can act as alternative promoters for nearby genes resulting in non-canonical regulation of transcription5,6. However, TE activity can lead to detrimental genome instability7, and hosts have evolved mechanisms to appropriately silence TE mobility8,9. Recent studies have demonstrated that a subset of TEs, endogenous retroviral elements (ERVs) containing long terminal repeats (LTRs), are silenced through trimethylation of histone H3 on lysine 9 (H3K9me3) by ESET (also known as SETDB1, SET domain bifurcated 1, or KMT1E)10 and a co-repressor complex containing KAP1 (KRAB-associated protein 1, also known as tripartite motif-containing protein 28, TRIM28)11 in mouse embryonic stem cells (ESCs). Here we show that the replacement histone variant H3.3 is enriched at class I and class II ERVs, notably early transposon (ETn)/MusD and intracisternal A-type particles (IAPs). Deposition at a subset of these elements is dependent upon the H3.3 chaperone complex containing ATRX (alpha thalesemia/mental retardation syndrome X)12 and DAXX (Death-associated protein 6)12-14. We demonstrate that recruitment of DAXX, H3.3, and KAP1 to ERVs are co-dependent and upstream of ESET, linking H3.3 to ERV-associated H3K9me3. Importantly, H3K9me3 is reduced at ERVs upon H3.3 deletion, resulting in derepression and dysregulation of adjacent, endogenous genes, along with increased retrotransposition of IAPs. Our study identifies a unique heterochromatin state marked by the presence of both H3.3 and H3K9me3 and establishes an important role for H3.3 in control of ERV retrotransposition in ESCs.

RNase L restricts the mobility of engineered retrotransposons in cultured human cells

Retrotransposons are mobile genetic elements, and their mobility can lead to genomic instability. Retrotransposon insertions are associated with a diverse range of sporadic diseases, including cancer. Thus, it is not a surprise that multiple host defense mechanisms suppress retrotransposition. The 2′,5′-oligoadenylate (2-5A) synthetase (OAS)-RNase L system is a mechanism for restricting viral infections during the interferon antiviral response. Here, we investigated a potential role for the OAS-RNase L system in the restriction of retrotransposons. Expression of wild type (WT) and a constitutively active form of RNase L (NΔ385), but not a catalytically inactive RNase L mutant (R667A), impaired the mobility of engineered human LINE-1 (L1) and mouse intracisternal A-type particle retrotransposons in cultured human cells. Furthermore, WT RNase L, but not an inactive RNase L mutant (R667A), reduced L1 RNA levels and subsequent expression of the L1-encoded proteins (ORF1p and ORF2p). Consistently, confocal immunofluorescent microscopy demonstrated that WT RNase L, but not RNase L R667A, prevented formation of L1 cytoplasmic foci. Finally, siRNA-mediated depletion of endogenous RNase L in a human ovarian cancer cell line (Hey1b) increased the levels of L1 retrotransposition by ∼2-fold. Together, these data suggest that RNase L might function as a suppressor of structurally distinct retrotransposons.

Visualized Computational Predictions of Transcriptional Effects by Intronic Endogenous Retroviruses

When endogenous retroviruses (ERVs) or other transposable elements (TEs) insert into an intron, the consequence on gene transcription can range from negligible to a complete ablation of normal transcripts. With the advance of sequencing technology, more and more insertionally polymorphic or private TE insertions are being identified in humans and mice, of which some could have a significant impact on host gene expression. Nevertheless, an efficient and low cost approach to prioritize their potential effect on gene transcription has been lacking. By building a computational model based on artificial neural networks (ANN), we demonstrate the feasibility of using machine-learning approaches to predict the likelihood that intronic ERV insertions will have major effects on gene transcription, focusing on the two ERV families, namely Intracisternal A-type Particle (IAP) and Early Transposon (ETn)/MusD elements, which are responsible for the majority of ERV-induced mutations in mice. We trained the ANN model using properties associated with these ERVs known to cause germ-line mutations (positive cases) and properties associated with likely neutral ERVs of the same families (negative cases), and derived a set of prediction plots that can visualize the likelihood of affecting gene transcription by ERV insertions. Our results show a highly reliable prediction power of our model, and offer a potential approach to computationally screen for other types of TE insertions that may affect gene transcription or even cause disease.

Env-less endogenous retroviruses are genomic superspreaders

Endogenous retroviruses (ERVs) differ from typical retroviruses in being inherited through the host germline and therefore are a unique combination of pathogen and selfish genetic element. Some ERV lineages proliferate by infecting germline cells, as do typical retroviruses, whereas others lack the env gene required for virions to enter cells and thus behave like retrotransposons. We wished to know what factors determined the relative abundance of different ERV lineages, so we analyzed ERV loci recovered from 38 mammal genomes by in silico screening. By modeling the relationship between proliferation and replication mechanism in detail within one group, the intracisternal A-type particles (IAPs), and performing simple correlations across all ERV lineages, we show that when ERVs lose the env gene their proliferation within that genome is boosted by a factor of ∼30. We also show that ERV abundance follows the Pareto principle or 20/80 rule, with ∼20% of lineages containing 80% of the loci. This rule is observed in many biological systems, including infectious disease epidemics, where commonly ∼20% of the infected individuals are responsible for 80% of onward infection. We thus borrow simple epidemiological and ecological models and show that retrotransposition and loss of env is the trait that leads endogenous retroviruses to becoming genomic superspreaders that take over a significant proportion of their host's genome.

The Mouse IAPE Endogenous Retrovirus Can Infect Cells through Any of the Five GPI-Anchored EphrinA Proteins

The IAPE (Intracisternal A-type Particles elements with an Envelope) family of murine endogenous retroelements is present at more than 200 copies in the mouse genome. We had previously identified a single copy that proved to be fully functional, i.e. which can generate viral particles budding out of the cell and infectious on a series of cells, including human cells. We also showed that IAPE are the progenitors of the highly reiterated IAP elements. The latter are now strictly intracellular retrotransposons, due to the loss of the envelope gene and re-localisation of the associated particles in the course of evolution. In the present study we searched for the cellular receptor of the IAPE elements, by using a lentiviral human cDNA library and a pseudotype assay on transduced cells. We identified Ephrin A4, a GPI-anchored molecule involved in several developmental processes, as a receptor for the IAPE pseudotypes. We also found that the other 4 members of the Ephrin A family –but not those of the closely related Ephrin B family- were also able to mediate IAPE cell entry, thus significantly increasing the amount of possible cell types susceptible to IAPE infection. We show that these include mouse germline cells, as illustrated by immunohistochemistry experiments, consistent with IAPE genomic amplification by successive re-infection. We propose that the uncovered properties of the identified receptors played a role in the accumulation of IAPE elements in the mouse genome, and in the survival of a functional copy.