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Social animals utilise various communication methods to organise their societies. In social insects, nestmate discrimination plays a crucial role in regulating colony membership. Counter to this system, socially parasitic species employ diverse behavioural and chemical strategies to bypass their host's detection. In this study, we tested whether such parasitic adaptations could be detected in the incipient stage of social parasitism that is observed as intraspecific phenomena in some social insects. The Japanese parthenogenetic ant Pristomyrmex punctatus harbours a genetically distinct cheater lineage which infiltrates and exploits host colonies. We found that intrusion of this intraspecific social parasite was defended by nestmate discrimination of host colonies without any behavioural strategies specialised in social parasitism. Most of the cheaters were eliminated through aggressions by host workers that are typically observed against non-nestmates, resulting in a low intrusion success rate for the cheaters (6.7%). This result contrasts with the expectation from interspecific social parasitism but rather resembles the intraspecific counterpart reported in Cape honeybees (Apis mellifera capensis), illustrating the role of nestmate discrimination against the intrusion of intraspecific social parasites.Competing Interest StatementThe authors have declared no competing interest.Footnotes* The entire manuscript was substantially rewritten, including the title change. Information about the study system was added in the introduction; Study design was clarified in Figure 1; statistical analyses and their visualization were totally revised to address mixed effect models.* https://doi.org/10.5061/dryad.59zw3r2h2

Background Subcellular localization of coding and non-coding RNAs has emerged as major regulatory mechanisms of gene expression in various cell types and many organisms. However, techniques that enable detection of the subcellular distribution of these RNAs with high sensitivity and high resolution remain limited, particularly in vertebrate adult tissues and organs. In this study, we examined the expression and localization of mRNAs encoding Pou5f1/Oct4, Mos, Cyclin B1 and Deleted in Azoospermia-like (Dazl) in zebrafish and mouse ovaries by combining tyramide signal amplification (TSA)-based in situ hybridization with paraffin sections which can preserve cell morphology of tissues and organs at subcellular levels. In addition, the distribution of a long non-coding RNA (lncRNA), lncRNA-HSVIII , in mouse testes was examined by the same method. Results The mRNAs encoding Mos, Cyclin B1 and Dazl were found to assemble into distinct granules that were distributed in different subcellular regions of zebrafish and mouse oocytes, suggesting conserved and specific regulations of these mRNAs. The lncRNA-HSVIII was first detected in the nucleus of spermatocytes at prophase I of the meiotic cell cycle and was then found in the cytoplasm of round spermatids, revealing expression patterns of lncRNA during germ cell development. Collectively, the in situ hybridization method demonstrated in this study achieved the detection and comparison of precise distribution patterns of coding and non-coding RNAs at subcellular levels in single cells of adult tissues and organs. Conclusions This high-sensitivity and high-resolution in situ hybridization is applicable to many vertebrate species and to various tissues and organs and will be useful for studies on the subcellular regulation of gene expression at the level of RNA localization.

We identify a dayside electron diffusion region (EDR) encountered by the Magnetospheric Multiscale (MMS) mission and estimate the terms in generalized Ohm's law that controlled energy conversion near the X-point. MMS crossed the moderate-shear (130 degrees) magnetopause southward of the exact X-point. MMS likely entered the magnetopause far from the X-point, outside the EDR, as the size of the reconnection layer was less than but comparable to the magnetosheath proton gyro-radius, and also as anisotropic gyrotropic \"outflow\" crescent electron distributions were observed. MMS then approached the X-point, where all four spacecraft simultaneously observed signatures of the EDR, e.g., an intense out-of-plane electron current, moderate electron agyrotropy, intense electron anisotropy, non-ideal electric fields, non-ideal energy conversion, etc. We find that the electric field associated with the non-ideal energy conversion is (a) well described by the sum of the electron inertial and pressure divergence terms in generalized Ohms law though (b) the pressure divergence term dominates the inertial term by roughly a factor of 5:1, (c) both the gyrotropic and agyrotropic pressure forces contribute to energy conversion at the X-point, and (d) both out-of-the-reconnection-plane gradients (d/dM) and in-plane (d/dL,N) in the pressure tensor contribute to energy conversion near the X-point. This indicates that this EDR had some electron-scale structure in the out-of-plane direction during the time when (and at the location where) the reconnection site was observed.