Literature DB >> 9806775

Gap junctions are involved in the early generation of left-right asymmetry.

M Levin1, M Mercola.   

Abstract

Invariant left-right asymmetry of the visceral organs is a fundamental feature of vertebrate embryogenesis. While a cascade of asymmetrically expressed genes has been described, the embryonic mechanism that orients the left-right axis relative to the dorsoventral and anteroposterior axes (a prerequisite for asymmetric gene expression) is unknown. We propose that this process involves dorsoventral differences in cell-cell communication through gap junctions composed of connexin proteins. Global modulation of gap junctional states in Xenopus embryos by pharmacological agents specifically induced heterotaxia involving mirror-image reversals of heart, gut, and gall bladder. Greatest sensitivity was observed between st. 5 and st. 12, well before the onset of organogenesis. Moreover, heterotaxia was also induced following microinjection of dominant negative and wild-type connexin mRNAs to modify the endogenous dorsoventral difference in junctional communication. Heterotaxia was induced by either blocking gap junction communication (GJC) dorsally or by introducing communication ventrally (but not the reverse). Both connexin misexpression and exposure to GJC-modifying drugs altered expression of the normally left-sided gene XNR-1, demonstrating that GJC functions upstream of XNR-1 in the pathway that patterns left-right asymmetry. Finally, lineage analysis to follow the progeny of microinjected cells indicated that they generally do not contribute the asymmetric organs. Together with the early sensitivity window, this suggests that GJC functions as part of a fundamental, early aspect of left-right patterning. In addition, we show that a potential regulatory mutation in Connexin43 is sufficient to cause heterotaxia. Despite uncertainty about the prevalence of the serine364 to proline substitution reported in human patients with laterality defects, the mutant protein is both a mild hypomorph and a potent antimorph as determined by the effect of its expression on left-right patterning. Taken together, our data suggest that endogenous dorsoventral differences in GJC within the early embryo are needed to consistently orient left-right asymmetry. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9806775     DOI: 10.1006/dbio.1998.9024

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  61 in total

1.  Gut endoderm is involved in the transfer of left-right asymmetry from the node to the lateral plate mesoderm in the mouse embryo.

Authors:  Ranajeet S Saund; Masami Kanai-Azuma; Yoshiakira Kanai; Injune Kim; Mary T Lucero; Yukio Saijoh
Journal:  Development       Date:  2012-05-23       Impact factor: 6.868

2.  The ATP-sensitive K(+)-channel (K(ATP)) controls early left-right patterning in Xenopus and chick embryos.

Authors:  Sherry Aw; Joseph C Koster; Wade Pearson; Colin G Nichols; Nian-Qing Shi; Katia Carneiro; Michael Levin
Journal:  Dev Biol       Date:  2010-07-17       Impact factor: 3.582

3.  An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesis.

Authors:  Ashley E Cast; Chunlei Gao; Jeffrey D Amack; Stephanie M Ware
Journal:  Dev Biol       Date:  2012-01-21       Impact factor: 3.582

Review 4.  Do we know anything about how left-right asymmetry is first established in the vertebrate embryo?

Authors:  Cliff Tabin
Journal:  J Mol Histol       Date:  2005-10-15       Impact factor: 2.611

5.  Inverse drug screens: a rapid and inexpensive method for implicating molecular targets.

Authors:  Dany S Adams; Michael Levin
Journal:  Genesis       Date:  2006-11       Impact factor: 2.487

Review 6.  Calcium at fertilization and in early development.

Authors:  Michael Whitaker
Journal:  Physiol Rev       Date:  2006-01       Impact factor: 37.312

7.  Early, H+-V-ATPase-dependent proton flux is necessary for consistent left-right patterning of non-mammalian vertebrates.

Authors:  Dany S Adams; Kenneth R Robinson; Takahiro Fukumoto; Shipeng Yuan; R Craig Albertson; Pamela Yelick; Lindsay Kuo; Megan McSweeney; Michael Levin
Journal:  Development       Date:  2006-03-22       Impact factor: 6.868

8.  The C-terminus of connexin43 adopts different conformations in the Golgi and gap junction as detected with structure-specific antibodies.

Authors:  Gina E Sosinsky; Joell L Solan; Guido M Gaietta; Lucy Ngan; Grace J Lee; Mason R Mackey; Paul D Lampe
Journal:  Biochem J       Date:  2007-12-15       Impact factor: 3.857

9.  KCNQ1 and KCNE1 K+ channel components are involved in early left-right patterning in Xenopus laevis embryos.

Authors:  Junji Morokuma; Douglas Blackiston; Michael Levin
Journal:  Cell Physiol Biochem       Date:  2008-04-24

Review 10.  A unified model for left-right asymmetry? Comparison and synthesis of molecular models of embryonic laterality.

Authors:  Laura N Vandenberg; Michael Levin
Journal:  Dev Biol       Date:  2013-04-10       Impact factor: 3.582

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