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哺乳动物是地球上适应能力最强的动物类群,可适应各种生境,具有动物界中最宽的生态幅,哺乳动物特有的皮肤衍生物——被毛,发挥了十分重要的作用,成为哺乳动物适应多种环境的重要手段。有关哺乳动物季节性换毛规律的研究,是动物生态学研究的一个重要方面,但目前相关研究少且文献较零散,缺乏系统的研究进展综述。本文从被毛的功能、被毛的生长、季节性换毛序规律以及影响哺乳动物季节性换毛的主要因素这4方面研究进行综述,探讨目前研究中存在的潜在问题,展望了哺乳动物季节性换毛规律的研究方法以及在全球变暖的大背景下,气候变化与动物物候之间的关系等方面的研究趋势,以期为未来继续深入研究哺乳动物季节性换毛规律提供一定的科学参考。

Molting is an important process in which old and worn feathers are exchanged for new ones. Plumage color is determined by pigments such as carotenes, melanin and by the ultrastructure of the feather. The importance of plumage coloration has been widely studied in different groups of birds, generally at a particular time of the year. However, plumage coloration is not static and few studies have addressed the change in plumage color over time and its relationship to reproductive tasks. The Eared Dove (Zenaida auriculata, Des Murs, 1847) has a melanistic coloration with sexual dichromatism in different body regions. The Eared Dove's crown is the most exposed body region during the bowing display. Our objective was therefore to accurately determine the molting period of the crown feathers and study the seasonal variation in their coloration in females and males. Our findings indicate a molting period of 6 months (January to June). The new feathers are undergoing changes in their coloration from July to December. During that period we apply an avian vision model then enabled us to reveal a seasonal variation in the coloration of the crown feathers in both sexes, as given by a change in the chromatic distances. The highest values in the chromatic distances towards the reproductive period are given by a change in the UV-violet component of the spectrum, indicating changes in the microstructure of the feather. This change in crown coloration towards the breeding season could be linked to reproductive behaviors.

Molt is a critical developmental process in crustaceans. Recent studies have shown that the hepatopancreas is an important source of innate immune molecules, yet hepatopancreatic patterns of gene expression during the molt cycle which may underlie changes in immune mechanism are unknown. In this study, we performed Illumina sequencing for the hepatopancreas of the mud crab, Scylla paramamosain during molt cycle (pre-molt stage, post-molt stage, and inter-molt stage). A total of 44.55 Gb high-quality reads were obtained from the normalized cDNA of hepatopancreas. A total of 70,591 transcripts were assembled; 55,167 unigenes were identified. Transcriptomic comparison revealed 948 differentially expressed genes (DEGs) in the hepatopancreas from the three molt stages. We found that genes associated with immune response patterns changed in expression during the molt cycle. Antimicrobial peptide genes, inflammatory response genes, Toll signaling pathway factors, the phenoloxidase system, antioxidant enzymes, metal-binding proteins and other immune related genes are significantly up-regulated at the post-molt stage and inter-molt stage compared with the pre-molt stage, respectively. These genes are either not expressed or are expressed at low levels at the pre-molt stage. To our knowledge, this is the first systematic transcriptome analysis of genes capable of mobilizing a hepatopancreas immune response during the molt cycle in crustaceans, and this study will contribute to a better understanding of the hepatopancreas immune system and mud crab prophylactic immune mechanisms at the post-molt stage.

Holometabolous insects stop feeding at the final larval instar stage and then undergo metamorphosis; however, the mechanism is unclear. In the present study, using the serious lepidopteran agricultural pest Helicoverpa armigera as a model, we revealed that 20-hydroxyecdysone (20E) binds to the dopamine receptor (DopEcR), a G protein-coupled receptor, to stop larval feeding and promote pupation. DopEcR was expressed in various tissues and its level increased during metamorphic molting under 20E regulation. The 20E titer was low during larval feeding stages and high during wandering stages. By contrast, the dopamine (DA) titer was high during larval feeding stages and low during the wandering stages. Injection of 20E or blocking dopamine receptors using the inhibitor flupentixol decreased larval food consumption and body weight. Knockdown of DopEcR repressed larval feeding, growth, and pupation. 20E, via DopEcR, promoted apoptosis; and DA, via DopEcR, induced cell proliferation. 20E opposed DA function by repressing DA-induced cell proliferation and AKT phosphorylation. 20E, via DopEcR, induced gene expression and a rapid increase in intracellular calcium ions and cAMP. 20E induced the interaction of DopEcR with G proteins αs and αq. 20E, via DopEcR, induced protein phosphorylation and binding of the EcRB1-USP1 transcription complex to the ecdysone response element. DopEcR could bind 20E inside the cell membrane or after being isolated from the cell membrane. Mutation of DopEcR decreased 20E binding levels and related cellular responses. 20E competed with DA to bind to DopEcR. The results of the present study suggested that 20E, via binding to DopEcR, arrests larval feeding and promotes pupation.

Biological rhythms regulate innumerable physiological processes, yet little is known of factors that regulate many of these rhythms. Disruption in the timing of these rhythms can have devastating impacts on population sustainability. We hypothesized that the timing of the molt infradian rhythm in the crustacean Daphnia magna is regulated by the joint action of the protein E75 and nitric oxide. Further, we hypothesized that disruption of the function of E75 would adversely impact several physiological processes related to growth and reproduction. Analysis of mRNA levels of several genes, involved in regulating the molt cycle in insects, revealed the sequential accumulation of E75, its dimer partner HR3, FTZ-F1, and CYP18a1 during the molt cycle. Exposure to the nitric oxide donor sodium nitroprusside early in the molt cycle had no effect on E75 or HR3 mRNA levels, but delayed the peak accumulation of FTZ-F1 and CYP18a1 mRNA. The subsequent exuviation was also delayed consistent with the delay in peak accumulation of FTZ-F1 and CYP18a1. These results supported our assertion that nitric oxide binds E75 rendering it incapable of binding HR3. Excess HR3 protein then enhanced the accumulation of the downstream products FTZ-F1 and CYP18a1. Similarly, suppression of E75 mRNA levels, using siRNA, had no effect on mRNA levels of HR3 but elevated mRNA levels of FTZ-F1. Consistent with these molecular responses, the suppression of E75 using siRNA increased the duration of the molt cycle and reduced the number of offspring produced. We conclude that the molt cycle of daphnids is regulated in a manner similar to insects and disruption of E75 results in a lengthening of the molt cycle and a reduction the release of viable offspring.

Molting is natural adaptation to climate change in all birds, including chickens. Forced molting (FM) can rejuvenate and reactivate the reproductive potential of aged hens, but the effect of natural molting (NM) on older chickens is not clear. To explore why FM has a dramatically different effect on chickens compared with NM, the transcriptome analyses of the hypothalamus and ovary in forced molted and natural molted hens at two periods with feathers fallen and regrown were performed. Additionally, each experimental chicken was tested for serological indices. The results of serological indices showed that growth hormone, thyroid stimulating hormone, and thyroxine levels were significantly higher (p < 0.05) in forced molted hens than in natural molted hens, and calcitonin concentrations were lower in the forced molted than in the natural molted hens. Furthermore, the transcriptomic analysis revealed a large number of genes related to disease resistance and anti-aging in the two different FM and NM periods. These regulatory genes and serological indices promote reproductive function during FM. This study systematically revealed the transcriptomic and serological differences between FM and NM, which could broaden our understanding of aging, rejuvenation, egg production, and welfare issues related to FM in chickens.

Ecdysis is a well-known developmental feature among arthropods. Because the aggregate and synchronous molting of first-instar scorpions is markedly different from the common independent molting behavior of older scorpions and most arthropods, knowledge on the biological benefits of the unusual behavior of first-instar scorpions remain limited. Before the molting of newborn scorpions, their mothers exhibited a remarkable ability to efficiently locate the fallen offspring and help them climb onto their back, which was supported by strong maternal behavior because they climbed more swiftly than the 7-day postpartum scorpions. Most newborn scorpions molted and survived on the mother’s back, with a survival rate of approximately 100%, and most newborn scorpions survived via aggregate molting behavior on sand in the absence of mothers (89.83% ± 1.91%). The important role of the mother scorpion was further highlighted in mothers with one to five first-instar scorpions. While all first-instar scorpions individually or reciprocally molted and survived on the mother’s back, only 52.00% ± 7.14% to 79.20% ± 4.24% of newborn scorpions isolated from the mother could individually or reciprocally molt and survive on the sand, and the aggregated states of first-instar scorpions strengthened as their numbers on sand increased before molting. These results highlight collaborative molting as an evolutionary driving force for newborn scorpions. Taken together, both maternal care and collaborative aggregate molting behavior enhanced the survival of first-instar scorpions before and after molting, and these benefits for first-instar scorpions play essential and evolutionary roles in scorpion survival.

Background The fertility of roosters significantly impacts the economic outcome of the poultry industry. However, it is common for some roosters to fail to produce semen during production, and the underlying reasons remain largely unclear. Results To investigate a solution to this problem, induced molting (IM) was performed on no-semen (NS) roosters. Remarkably, the NS roosters recovered and began producing semen on 30 d after recovery feeding (R30), with semen quality and ejaculation volume returning to normal levels by 39 days after recovery feeding (R39). The difference in testicular weight between the NS and healthy roosters was significant on one day before fasting (F0) ( P  < 0.05). Meanwhile, morphological analysis of NS roosters’ testicular seminiferous tubules suggested that Sertoli cells (SCs), which form the scaffold in the testicular microenvironment, were severely damaged in NS roosters. Their spermatogenic cells were disordered and fewer, suggesting abnormal testicular function in NS roosters. Following induced molting, the epithelial structure of seminiferous tubules in the testes of NS roosters was restored, and follicle-stimulating hormone (FSH) levels in both serum and testicular were significantly higher ( P  < 0.05). To further elucidate the mechanisms, transcriptome analysis was conducted to uncover dynamic gene expression changes in testicular tissues at two time points: F0 and R39. Results indicated that ALDH1A1 levels in the testes of NS roosters were 16.0-fold lower than those in healthy roosters at F0 but significantly increased by R39, suggesting that the ALDH1A1 gene may be closely related to testicular failure in NS roosters. Pathway-enrichment analyses revealed that IM significantly activated the phagosome pathway in the testes of NS roosters, and the genes ATP6VOD2,ATP6V1A,Ighm and MHCY2B1 were involved in this pathway, associated with autophagy. We hypothesize that in response to nutrient deprivation, autophagy is initiated to degrade damaged components in the seminiferous tubules of NS roosters, leading to testicular physiological remodeling and resumption of semen production. Conclusions This report identifies critical pathway and molecular markers related to testicular failure and physiological remodeling in NS roosters caused by induced molting, offering an essential reference for accelerating genetic selection.