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Diaphanous gene mutation affects spiral cleavage and chirality in snails

L-R (left and right) symmetry breaking during embryogenesis and the establishment of asymmetric body plan are key issues in developmental biology, but the onset including the handedness-determining gene locus still remains unknown. Using pure dextral (DD) and sinistral (dd) strains of the pond snail...

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Autores principales: Kuroda, Reiko, Fujikura, Kohei, Abe, Masanori, Hosoiri, Yuji, Asakawa, Shuichi, Shimizu, Miho, Umeda, Shin, Ichikawa, Futaba, Takahashi, Hiromi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052593/
https://www.ncbi.nlm.nih.gov/pubmed/27708420
http://dx.doi.org/10.1038/srep34809
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author Kuroda, Reiko
Fujikura, Kohei
Abe, Masanori
Hosoiri, Yuji
Asakawa, Shuichi
Shimizu, Miho
Umeda, Shin
Ichikawa, Futaba
Takahashi, Hiromi
author_facet Kuroda, Reiko
Fujikura, Kohei
Abe, Masanori
Hosoiri, Yuji
Asakawa, Shuichi
Shimizu, Miho
Umeda, Shin
Ichikawa, Futaba
Takahashi, Hiromi
author_sort Kuroda, Reiko
collection PubMed
description L-R (left and right) symmetry breaking during embryogenesis and the establishment of asymmetric body plan are key issues in developmental biology, but the onset including the handedness-determining gene locus still remains unknown. Using pure dextral (DD) and sinistral (dd) strains of the pond snail Lymnaea stagnalis as well as its F(2) through to F(10) backcrossed lines, the single handedness-determining-gene locus was mapped by genetic linkage analysis, BAC cloning and chromosome walking. We have identified the actin-related diaphanous gene Lsdia1 as the strongest candidate. Although the cDNA and derived amino acid sequences of the tandemly duplicated Lsdia1 and Lsdia2 genes are very similar, we could discriminate the two genes/proteins in our molecular biology experiments. The Lsdia1 gene of the sinistral strain carries a frameshift mutation that abrogates full-length LsDia1 protein expression. In the dextral strain, it is already translated prior to oviposition. Expression of Lsdia1 (only in the dextral strain) and Lsdia2 (in both chirality) decreases after the 1-cell stage, with no asymmetric localization throughout. The evolutionary relationships among body handedness, SD/SI (spiral deformation/spindle inclination) at the third cleavage, and expression of diaphanous proteins are discussed in comparison with three other pond snails (L. peregra, Physa acuta and Indoplanorbis exustus).
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spelling pubmed-50525932016-10-19 Diaphanous gene mutation affects spiral cleavage and chirality in snails Kuroda, Reiko Fujikura, Kohei Abe, Masanori Hosoiri, Yuji Asakawa, Shuichi Shimizu, Miho Umeda, Shin Ichikawa, Futaba Takahashi, Hiromi Sci Rep Article L-R (left and right) symmetry breaking during embryogenesis and the establishment of asymmetric body plan are key issues in developmental biology, but the onset including the handedness-determining gene locus still remains unknown. Using pure dextral (DD) and sinistral (dd) strains of the pond snail Lymnaea stagnalis as well as its F(2) through to F(10) backcrossed lines, the single handedness-determining-gene locus was mapped by genetic linkage analysis, BAC cloning and chromosome walking. We have identified the actin-related diaphanous gene Lsdia1 as the strongest candidate. Although the cDNA and derived amino acid sequences of the tandemly duplicated Lsdia1 and Lsdia2 genes are very similar, we could discriminate the two genes/proteins in our molecular biology experiments. The Lsdia1 gene of the sinistral strain carries a frameshift mutation that abrogates full-length LsDia1 protein expression. In the dextral strain, it is already translated prior to oviposition. Expression of Lsdia1 (only in the dextral strain) and Lsdia2 (in both chirality) decreases after the 1-cell stage, with no asymmetric localization throughout. The evolutionary relationships among body handedness, SD/SI (spiral deformation/spindle inclination) at the third cleavage, and expression of diaphanous proteins are discussed in comparison with three other pond snails (L. peregra, Physa acuta and Indoplanorbis exustus). Nature Publishing Group 2016-10-06 /pmc/articles/PMC5052593/ /pubmed/27708420 http://dx.doi.org/10.1038/srep34809 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kuroda, Reiko
Fujikura, Kohei
Abe, Masanori
Hosoiri, Yuji
Asakawa, Shuichi
Shimizu, Miho
Umeda, Shin
Ichikawa, Futaba
Takahashi, Hiromi
Diaphanous gene mutation affects spiral cleavage and chirality in snails
title Diaphanous gene mutation affects spiral cleavage and chirality in snails
title_full Diaphanous gene mutation affects spiral cleavage and chirality in snails
title_fullStr Diaphanous gene mutation affects spiral cleavage and chirality in snails
title_full_unstemmed Diaphanous gene mutation affects spiral cleavage and chirality in snails
title_short Diaphanous gene mutation affects spiral cleavage and chirality in snails
title_sort diaphanous gene mutation affects spiral cleavage and chirality in snails
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052593/
https://www.ncbi.nlm.nih.gov/pubmed/27708420
http://dx.doi.org/10.1038/srep34809
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