Literature DB >> 20040754

Methods for karyotyping and for localization of developmentally relevant genes on the chromosomes of the purple sea urchin, Strongylocentrotus purpuratus.

Celeste C Eno1, Stefanie A Böttger, Charles W Walker.   

Abstract

The purple sea urchin, Strongylocentrotus purpuratus, is the only non-chordate deuterostome model with a fully sequenced genome. Chromosomal localization of individual genes and resulting gene maps are unavailable for this or for any sea urchin. As a result, the purple sea urchin genome has not been mapped onto specific chromosomes and remains inaccessible to genome-wide approaches addressing questions that require positional information for particular genes. Here we describe the first successful methods for karyotyping and localizing specific gene loci on chromosomes of Strongylocentrotus purpuratus and those of the phylogenetically related Strongylocentrotus droebachiensis. Both species have 42 chromosomes in their diploid genomes (n = 21). There are 2 large, 8 medium, and 10 small pairs, plus one putative sex pair. In both species, bindin genes were localized to 2 pair of homologous chromosomes by fluorescent in situ hybridization. Fluorescently labeled bacterial artificial chromosome clones generated from S. purpuratus for the functionally related genes brachyury, foxa, and foxb were localized to different chromosomes. Our protocols provide previously unavailable tools for developing a gene map for the purple sea urchin genome.

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Year:  2009        PMID: 20040754     DOI: 10.1086/BBLv217n3p306

Source DB:  PubMed          Journal:  Biol Bull        ISSN: 0006-3185            Impact factor:   1.818


  4 in total

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Authors:  Quanchao Wang; Ying Liu; Yanxia Wang; Shaoyu Jiang; Chuanxin Zhang; Baoquan Li
Journal:  Mar Biotechnol (NY)       Date:  2021-11-23       Impact factor: 3.619

2.  Current Status of Echinoderm Genome Analysis - What do we Know?

Authors:  Mariko Kondo; Koji Akasaka
Journal:  Curr Genomics       Date:  2012-04       Impact factor: 2.236

3.  The Spindle Assembly Checkpoint Functions during Early Development in Non-Chordate Embryos.

Authors:  Janet Chenevert; Marianne Roca; Lydia Besnardeau; Antonella Ruggiero; Dalileh Nabi; Alex McDougall; Richard R Copley; Elisabeth Christians; Stefania Castagnetti
Journal:  Cells       Date:  2020-04-28       Impact factor: 6.600

4.  Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family.

Authors:  Matan Oren; Megan A Barela Hudgell; Brian D'Allura; Jacob Agronin; Alexandra Gross; Daniele Podini; L Courtney Smith
Journal:  BMC Genomics       Date:  2016-11-09       Impact factor: 3.969

  4 in total

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