Literature DB >> 17963275

Circadian clocks during embryonic and fetal development.

Maria Seron-Ferre1, Gullermo J Valenzuela, Claudia Torres-Farfan.   

Abstract

Circadian rhythmicity is a fundamental characteristic of organisms, which helps ensure that vital functions occur in an appropriate and precise temporal sequence and in accordance with cyclic environmental changes. Living beings are endowed with a system of biological clocks that measure time on a 24-hr basis, termed the circadian timing system. In mammals, the system is organized as a master clock located in the suprachiasmatic nucleus (SCN) of the hypothalamus, commanding peripheral clocks located in almost every tissue of the body. At the cell level, interlocking transcription/translation feedback loops of the genes Bmal-1, Clock, Per1-2, and Cry1-2, named clock genes, and their protein products results in circadian oscillation of clock genes and of genes involved in almost every cellular function. During gestation, the conceptus follows a complex and dynamic program by which it is simultaneously fit to develop and live in a circadian environment provided by its mother and to prepare for the very different environment that it will experience after birth. It has been known for a number of years that the mother tells the fetus the time of day and season of the year, and that the fetus uses this information to set the phase of fetal and neonatal circadian rhythms. There is evidence that the maternal rhythm of melatonin is one of the time signals to the fetus. In the last few years, the study of the development of the circadian system has turned to the investigation of the oscillatory expression of clock genes and their possible role in development, and to answering questions on the organization of the fetal circadian system. Emerging evidence shows that clock genes are expressed in the oocyte and during early and late development in embryo/fetal organs in the rat and in a fetal primate. The data available raise the intriguing possibility that the fetal SCN and fetal tissues may be peripheral clocks commanded by separate maternal signals. The rapid methodological and conceptual advances on chronobiology may help to unravel how the developing embryo and fetus faces time in this plastic period of life. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17963275     DOI: 10.1002/bdrc.20101

Source DB:  PubMed          Journal:  Birth Defects Res C Embryo Today        ISSN: 1542-975X


  27 in total

1.  Epigenomics: maternal high-fat diet exposure in utero disrupts peripheral circadian gene expression in nonhuman primates.

Authors:  Melissa Suter; Philip Bocock; Lori Showalter; Min Hu; Cynthia Shope; Robert McKnight; Kevin Grove; Robert Lane; Kjersti Aagaard-Tillery
Journal:  FASEB J       Date:  2010-11-19       Impact factor: 5.191

Review 2.  Circuit development in the master clock network of mammals.

Authors:  Vania Carmona-Alcocer; Kayla E Rohr; Deborah A M Joye; Jennifer A Evans
Journal:  Eur J Neurosci       Date:  2018-12-05       Impact factor: 3.386

3.  Circadian clocks in rat skin and dermal fibroblasts: differential effects of aging, temperature and melatonin.

Authors:  Cristina Sandu; Taole Liu; André Malan; Etienne Challet; Paul Pévet; Marie-Paule Felder-Schmittbuhl
Journal:  Cell Mol Life Sci       Date:  2015-01-07       Impact factor: 9.261

4.  Maternal eating behavior is a major synchronizer of fetal and postnatal peripheral clocks in mice.

Authors:  Laurence Canaple; Aline Gréchez-Cassiau; Franck Delaunay; Ouria Dkhissi-Benyahya; Jacques Samarut
Journal:  Cell Mol Life Sci       Date:  2018-05-26       Impact factor: 9.261

5.  Gestational chronodisruption leads to persistent changes in the rat fetal and adult adrenal clock and function.

Authors:  E R Salazar; H G Richter; C Spichiger; N Mendez; D Halabi; K Vergara; I P Alonso; F A Corvalán; C Azpeleta; M Seron-Ferre; C Torres-Farfan
Journal:  J Physiol       Date:  2018-09-17       Impact factor: 5.182

6.  Light and melatonin schedule neuronal differentiation in the habenular nuclei.

Authors:  Nancy Hernandez de Borsetti; Benjamin J Dean; Emily J Bain; Joshua A Clanton; Robert W Taylor; Joshua T Gamse
Journal:  Dev Biol       Date:  2011-08-05       Impact factor: 3.582

7.  Prenatal maternal pesticide exposure in relation to sleep health of offspring during adolescence.

Authors:  Astrid N Zamora; Deborah J Watkins; Karen E Peterson; Martha M Téllez-Rojo; Howard Hu; John D Meeker; Alejandra Cantoral; Adriana Mercado-García; Erica C Jansen
Journal:  Environ Res       Date:  2021-08-29       Impact factor: 6.498

8.  Dysregulation of Npas2 leads to altered metabolic pathways in a murine knockout model.

Authors:  Derek O'Neil; Hector Mendez-Figueroa; Toni-Ann Mistretta; Chunliu Su; Robert H Lane; Kjersti M Aagaard
Journal:  Mol Genet Metab       Date:  2013-09-05       Impact factor: 4.797

9.  An investigation of fetal behavioural states during maternal sleep in healthy late gestation pregnancy: an observational study.

Authors:  Peter R Stone; Wendy Burgess; Jordan McIntyre; Alistair J Gunn; Christopher A Lear; Laura Bennet; Edwin A Mitchell; John M D Thompson
Journal:  J Physiol       Date:  2017-11-02       Impact factor: 5.182

10.  MT3 melatonin binding site, MT1 and MT2 melatonin receptors are present in oocyte, but only MT1 is present in bovine blastocyst produced in vitro.

Authors:  Rafael V Sampaio; Stefanne Dhúllia B Conceição; Moysés S Miranda; Lucia de Fatima S Sampaio; Otávio Mitio Ohashi
Journal:  Reprod Biol Endocrinol       Date:  2012-12-03       Impact factor: 5.211

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