86 research outputs found

    Structural and RNAi characterization of the German cockroach lipophorin receptor, and the evolutionary relationships of lipoprotein receptors

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    This article is available from: http://www.biomedcentral.com/1471-2199/8/53[Background] Lipophorin receptors (LpRs) have been described in a number of insects, but functional studies have been reported only in locusts and mosquitoes. The aim of the present work was to characterize the LpR of the cockroach Blattella germanica, not only molecularly but also functionally using RNAi techniques, and to place LpRs in a phylogenetical context among lipoprotein receptors.[Results] We cloned a putative LpR from B. germanica (BgLpR) using RT-PCR methods. Two isoforms of BgLpR that differ from each other by an insertion/deletion of 24 amino acids were obtained from the fat body and the ovary. A phylogenetical analysis of lipoprotein receptors showed that BgLpR grouped with other sequences annotated as LpR in a cluster placed as a sister group of vertebrate low density lipoprotein receptors (LDLR) + lipoprotein receptor-related proteins 8 (LPR8) + vitellogenin receptors (VgR) + very low density lipoprotein receptors (VLDLR). The two BgLpR isoforms are expressed in different adult female tissues (fat body, ovary, brain, midgut, muscle) and in embryos. In ovaries and fat body, the two isoforms are similarly expressed during the first gonadotrophic cycle. mRNA levels in the fat body increase in parallel to vitellogenesis, whereas they decrease in the ovaries. BgLpR protein levels increase in parallel to vitellogenesis in both organs. Treatment with juvenile hormone increases BgLpR protein. RNAi experiments show that females with lower BgLpR expression have less lipophorin in the growing oocytes with respect to controls.[Conclusion] The two isoforms of BgLpR are structurally similar to other LpRs. Phylogenetical analyses show that LpRs and the group formed by vertebrate LDLR + LPR8 + VgR + VLDLR, diverged from a common ancestor and diversified in parallel. The different expression patterns in the fat body and the ovary, comparing mRNA and protein, indicate that the corresponding mechanisms regulating BgLpR expression are different. Experiments with JH III suggest that such a hormone regulates the expression of BgLpR posttranscriptionally. RNAi experiments indicate that BgLpR is a functional lipophorin receptor.Financial support from the Ministry of Education and Science, Spain (projects BOS2002-03359, BFU2005-00264, AGL2002-01169, AGL2005- 00773) and the Generalitat de Catalunya (2001 SGR 003245) is gratefully acknowledged. L.C. is recipient of pre-doctoral research grants (I3P) from CSIC. We thank Prof. Coby Schal (North Carolina State University) for generous gifts of anti-lipophorin antibody.Peer reviewe

    Juvenile Hormone Titer Versus Juvenile Hormone Synthesis in Female Nymphs and Adults of the German Cockroach, Blattella germanica

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    Patterns of juvenile hormone have been intensively studied in the cockroach Blattella germanica under different physiological situations. However, data have been mainly obtained in vitro, and refer to hormone synthesized by isolated corpora allata, whereas information available on hormone concentration in the hemolymph is restricted to adult females. In order to complement our studies in vitro, we have measured juvenile hormone titer in the hemolymph of B. germanica females in four characteristic physiological situations: penultimate and last instar nymphs, adults during the first vitellogenic cycle, and adults transporting egg cases (ootheca). In general, a significant positive correlation between rates of hormone synthesis and concentration in the hemolymph is observed. The main disparities appear in the penultimate day of the period of ootheca transport, where titer is high whereas synthesis is low, and on day 6 of the first vitellogenic cycle, where synthesis increases whereas titer decreases. At these stages, the observed disparities between synthesis and titer might be explained by differential action of degradation enzymes

    Oogenesis in the cockroach Blattella germanica. Fine tunning by miRNA

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    Conferencia invitada al V International Simposium of Developmental Biology celebrado en Ribeirão Preto (Brasil) entre el 18 y el 21 de noviembre de 2011.Peer Reviewe

    The extracellular matrix protein SPARG is induced by juvenile hormone to regulate the dynamics of follicular cells during insect ovary maturation

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    Trabajo presentado en la 10th International Conference on Juvenile Hormones (JHX 2014), celebrada en Tsukuba (Japón) del 9 al 13 de junio de 2014.N

    La maduración del oocito en insectos. ¿Cómo se regula la oogénesis en las distintas especies?

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    Trabajo presentado en el V Congreso de la Sociedad Española de Biología Evolutiva (SESBE 2016), celebrado en Murcia del 18 al 21 de enero de 2016.La formación y maduración del oocito es un proceso altamente controlado, ya que todos los acontecimientos deben ocurrir en el momento adecuado y en la secuencia correcta para que la posterior embriogénesis se realice correctamente. En insectos se distinguen dos modelos de ovario, los que tienen ovariolos de tipo panoístico y los que los tienen de tipo meroístico, más modificado. El ovario panoístico no sólo lo encontramos en insectos, sino que es el tipo más común en la mayoría de especies de invertebrados y vertebrados. Muchos de los genes que se expresan en ovarios y controlan procesos básicos, como la polaridad del oocito o la proliferación de las células germinales y de las células somáticas, están altamente conservados en las distintas especies de insectos, tanto si muestran el ovario panoístico como el meroístico, pero los mecanismos de regulación pueden ser diferentes en uno y otro. El estudio de estos mecanismos en una especie como Blattella germanica, con ovarios panoísticos, comparándolos con los de especies con ovarios meroísticos muy bien conocidas, como Drosophila melanogaster, nos permitirá reconstruir los cambios evolutivos que han pro piciado la transición de un modelo de ovario a otro.N

    Modificación genética. Investigación para el control de Blatella germanica

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    Trabajo presentado en EXPOCIDA IBERIA 2020 (Congreso Profesional y Feria de Control de Plagas y Sanidad Ambiental), celebrado en Madrid el 20 y 21 de febrero de 2020.Utilización de herramientas moleculares para su posible uso en el control de plagas: el RNAi y el CRISPR-Cas9. Avances y estado actual de las investigaciones en CRISPR-Cas9 en el laboratorio y posibilidades futuras de uso en el control de cucarachas

    Regulation of insect oogenesis. More than an endocrine interplay

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    Trabajo presentado en la 28th Conference of European Comparative Endocrinologists (CECE 2016), celebrado en Lovaina del 21 al 25 de agosto de 2016.Oogenesis is a crucial process in the animal kingdom to ensure the continuity of the species. Thus, it is not surprising that it is finely regulated. During the process of oogenesis, the ovarian follicle gets a series of signals that initiates competence, which will ultimately lead to maturation and oviposition. Insects are good models to study oogenesis as they have developed very different strategies to regulate it, and one of the most basic has been the design of different ovarian types. Two main types can be distinguished among insects: the panoistic and the meroistic. The panoistic is common in phylogenetically basal species, whereas the meroistic type predominates in distal insect groups. To study insect oogenesis we currently use the cockroach Blattella germanica as a model , a basal species with panoistic ovaries. The knowledge of this species can allow comparing its oogenesis with that of more mo dified species, like Drosophila melanogaster (with meroistic ovaries). In B. germanica , the juvenile hormone is the main reproductive hormone, involved in vitellogenesis control and oocyte maturation. We will review the role of juvenile hormone and its sig naling pathway, the function of ecdysone, which is necessary for chorion formation in adult cockroaches, and is also involved in the first steps of oogenesis, and the role of the Insulin pathway, which regulates tissue growth as well as vitellogenesis thro ugh the control of juvenile hormone synthesis. Finally, we will comment the involvement of these hormones in the signaling pathways (Hippo, Notch) that typically regulate insect oogenesis, in general.N

    Role of capicua in oogenesis of panoistic ovaries

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    Trabajo presentado en la 4th Meeting of the Spanish Society of the Evolutionary Biology (SESBE 2013) celebrada en Barcelona del 27 al 29 de noviembre de 2013.N

    Ecdysone signalling and ovarian development in insects: From stem cells to ovarian follicle formation

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    © 2014 Elsevier B.V. Although a great deal of information is available concerning the role of ecdysone in insect oogenesis, research has tended to focus on vitellogenesis and choriogenesis. As such, the study of oogenesis in a strict sense has received much less attention. This situation changed recently when a number of observations carried out in the meroistic polytrophic ovarioles of Drosophila melanogaster started to unravel the key roles played by ecdysone in different steps of oogenesis. Thus, in larval stages, a non-autonomous role of ecdysone, first in repression and later in activation, of stem cell niche and primordial germ cell differentiation has been reported. In the adult, ecdysone stimulates the proliferation of germline stem cells, plays a role in stem cell niche maintenance and is needed non-cell-autonomously for correct differentiation of germline stem cells. Moreover, in somatic cells ecdysone is required for 16-cell cyst formation and for ovarian follicle development. In the transition from stages 8 to 9 of oogenesis, ecdysone signalling is fundamental when deciding whether or not to go ahead with vitellogenesis depending on the nutritional status, as well as to start border cell migration. This article is part of a Special Issue entitled: Nuclear receptors in animal development.Financial support for the work was provided by the Spanish MICINN (grant CGL2008-03517/BOS to XB) and MINECO (grants nos. CGL2012-36251 to XB and BFU2011-22404 to MDP), and from the Catalan Government (2009 SGR 1498). The research has also benefited from FEDER funds.Peer Reviewe
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