EXPRESS: Adults’ Responses to Infant Faces: Neutral Infant Facial Expressions Elicit the Strongest Baby Schema Effect

The effect of the babyface schema includes three typical responses, namely, the preference response, viewing motivation, and attention bias towards infant faces. It has been theorized that these responses are primarily influenced by infants’ facial structures. However, recent studies have revealed the moderating role of facial expression, suggesting that the strongest effect of the babyface schema may be related to the neutral facial expression; this hypothesis remains to be tested. In this study, the moderating role of facial expression was assessed in three successive experiments (total N = 402). We used a series of images of the same face with multiple expression-standardized images of infants and adults to control for facial structure. The results indicated that the effect sizes of the babyface schema (i.e., response differences between infants and adults) were different for multiple expressions of the same face. Specifically, the effect sizes of neutral faces were significantly greater than those of happy and sad faces according to the preference response (experiment 1, N = 90), viewing motivation (experiment 2, N = 214), and attentional bias (experiment 3, N = 98). These results empirically confirm that neutral infant facial expressions elicit the strongest effect of the babyface schema under the condition of using adult faces as a comparison baseline and matching multiple expressions of the same face.

Derivation and Interpretation of Expressiveness Devices in North Hail Arabic: Minimalist Account

This paper investigates the interpretive properties of what are termed expressiveness devices, characterised as clitic, pronoun and demonstrative. In what seems to be cases of multiple expression of a single argument, the proposed investigation involves generative syntactic analyses to the interaction of a set of expressiveness devices with an associate DP, accounting for their interpretation at both LF and PF interfaces (Chomsky, 1995 et seq). Exploration of a set of North Hail Arabic (henceforth, NHA) data containing expressiveness devices, all of which agree in φ-features with the associate DP, it is shown that the expressiveness devices maintain rigid order in the left periphery of the clause, each generated for certain discourse-interpretive property expressing a distinct value of information structure, through establishing an Agree relation (Chomsky, 2001) with the associate DP. Amongst the insights the analyses show is that NHA allows for multiple probes agreeing with a single goal. In this way, a probing head probes through another c-commanded probing head, in which case the goal is visible to the upper probing head. Movement is therefore shown to be triggered in case where goal’s visibility, related to feature valuation, is not available, hence, movement presupposes agreement.

A modular cloning toolkit for genome editing in plants

BackgroundCRISPR/Cas has recently become a widely used genome editing tool in various organisms, including plants. Applying CRISPR/Cas often requires delivering multiple expression units into plant and hence there is a need for a quick and easy cloning procedure. The modular cloning (MoClo), based on the Golden Gate (GG) method, has enabled development of cloning systems with standardised genetic parts, e.g. promoters, coding sequences or terminators, that can be easily interchanged and assembled into expression units, which in their own turn can be further assembled into higher order multigene constructs.ResultsHere we present an expanded cloning toolkit that contains ninety-nine modules encoding a variety of CRISPR/Cas-based nucleases and their corresponding guide RNA backbones. Among other components, the toolkit includes a number of promoters that allow expression of CRISPR/Cas nucleases (or any other coding sequences) and their guide RNAs in monocots and dicots. As part of the toolkit, we present a set of modules that enable quick and facile assembly of tRNA-sgRNA polycistronic units without a PCR step involved. We also demonstrate that our tRNA-sgRNA system is functional in wheat protoplasts.ConclusionsWe believe the presented CRISPR/Cas toolkit is a great resource that will contribute towards wider adoption of the CRISPR/Cas genome editing technology and modular cloning by researchers across the plant science community.

Enhancer Trapping and Annotation in Zebrafish Mediated with Sleeping Beauty, piggyBac and Tol2 Transposons

Although transposon-mediated enhancer trapping (ET) is successfully applied in diverse models, the efficiency of various transposon systems varies significantly, and little information is available regarding efficiency of enhancer trapping by various transposons in zebrafish. Most potential enhancers (Ens) still lack evidence of actual En activity. Here, we compared the differences in ET efficiency between sleeping beauty (SB), piggyBac (PB) and Tol2 transposons. Tol2 represented the highest germline transfer efficiencies at 55.56% (NF0 = 165), followed by SB (38.36%, NF0 = 151) and PB (32.65%, NF0 = 149). ET lines generated by the Tol2 transposon tended to produce offspring with a single expression pattern per line, while PB and SB tended to generate embryos with multiple expression patterns. In our tests, 10 putative Ens (En1–10) were identified by splinkerette PCR and comparative genomic analysis. Combining the GFP expression profiles and mRNA expression patterns revealed that En1 and En2 may be involved in regulation of the expression of dlx1a and dlx2a, while En6 may be involved in regulation of the expression of line TK4 transgene and rps26, and En7 may be involved in the regulation of the expression of wnt1 and wnt10b. Most identified Ens were found to be transcribed in zebrafish embryos, and their regulatory function may involve eRNAs.

Efficient Heterologous Production of Rhizopus oryzae Lipase via Optimization of Multiple Expression-Related Helper Proteins

This study is dedicated to efficiently produce Rhizopus oryzae lipase (ROL) by optimizing the expression of multiple expression-related helper proteins in Pichia pastoris. A series of engineered strains harboring different copy numbers of the ROL gene and different copies of the chaperone Pdi gene were first constructed to examine the influence of Pdi gene copy number on ROL production. The results showed that multiple copies of Pdi gene did not significantly improve ROL expression. Then, the effect of the co-overexpression of 10 expression-related helper proteins on ROL secretion was investigated by screening 20 colonies of each transformants. The data from shaking-flask fermentation suggested that Ssa4, Bmh2, Sso2, Pdi, Bip, Hac1, and VHb had positive effects on ROL expression. Subsequently, Ssa4, Bmh2, and Sso2, which all participate in vesicular trafficking and strongly promote ROL expression, were combined to further improve ROL production level. ROL activity of the screened strain GS115/5ROL-Ssa4-Sso2-Bmh2 4# attained 5230 U/mL. Furthermore, when the helper proteins Pdi, Bip, Hac1, and VHb were individually co-expressed with ROL in the strain GS115/5ROL-Ssa4-Sso2-Bmh2 4#, lipase activity increased to 5650 U/mL in the strain GS115/5ROL-Ssa4-Sso2-Bmh2-VHb 9#. Additionally, the maximum ROL activity of 41,700 U/mL was achieved in a 3 L bioreactor for high-density fermentation via a sorbitol–methanol co-feeding strategy, reaching almost twofold the value of the initial strain GS115/pAOα-5ROL 11#. Thus, the strategies in this study significantly increased ROL expression level, which is of great potential for the large-scale production of ROL in P. pastoris.