Literature DB >> 10603080

Conservation of the WD-repeat, microtubule-binding protein, EMAP, in sea urchins, humans, and the nematode C. elegans.

K A Suprenant1, J A Tuxhorn, M A Daggett, D P Ahrens, A Hostetler, J M Palange, C E VanWinkle, B T Livingston.   

Abstract

The echinoderm microtubule-associated protein (EMAP) is the most abundant microtubule-binding protein in the first cleavage mitotic apparatus in sea urchin embryos. The first goal of this study was to determine whether there is sufficient EMAP in the egg and embryo to modify microtubule dynamics during the early cleavages divisions and whether EMAP functions at a specific time or place in the embryo. To accomplish this goal, we examined the relative abundance, tissue distribution, and temporal pattern of EMAP expression during embryonic development. The second goal of this study was to identify important functional domains within the EMAP coding sequence. A conserved sequence might reveal a potential microtubule-binding domain. We cloned, sequenced and compared overlapping EMAP cDNAs from two different sea urchin species that diverged approximately 80 million years ago, and compared these with cDNA sequences from a vertebrate and nematode species. From quantitative immunoblots, we determined the EMAP concentration in eggs to be 4 microM. The steady-state levels of EMAP mRNA and protein accumulated during development, and all three germ layers expressed EMAP. During the early stages of development, EMAP and tubulin were both abundant in the ectoderm, mesoderm and endoderm. However, during late gastrulation and the formation of the early pluteus larvae, EMAP was enriched in the mesoderm, while tubulin staining was most abundant in the archenteron. These results indicate that EMAP may have tissue-specific functions in the late stage embryo. To identify conserved functional domains, we compared the predicted amino acid sequence encoded by Strongylocentrotus purpuratus and Lytechinus variegatus EMAP cDNAs, and determined that these two sea urchin EMAPs were 95% conserved and shared an identical domain organization. A parsimonious analysis of these sea urchin protein sequences, as well as human and C. elegans EMAP sequences was used to construct a gene tree. Together these results suggest that EMAP is an important microtubule protein required at all developmental stages of sea urchins, and whose cellular function may be conserved amongst metazoans.

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Year:  2000        PMID: 10603080     DOI: 10.1007/pl00008183

Source DB:  PubMed          Journal:  Dev Genes Evol        ISSN: 0949-944X            Impact factor:   0.900


  9 in total

1.  EML4 promotes the loading of NUDC to the spindle for mitotic progression.

Authors:  Dan Chen; Satoko Ito; Hong Yuan; Toshinori Hyodo; Kenji Kadomatsu; Michinari Hamaguchi; Takeshi Senga
Journal:  Cell Cycle       Date:  2015       Impact factor: 4.534

2.  Analysis of cytoskeletal and motility proteins in the sea urchin genome assembly.

Authors:  R L Morris; M P Hoffman; R A Obar; S S McCafferty; I R Gibbons; A D Leone; J Cool; E L Allgood; A M Musante; K M Judkins; B J Rossetti; A P Rawson; D R Burgess
Journal:  Dev Biol       Date:  2006-08-26       Impact factor: 3.582

3.  A Non-Synonymous Point Mutation in a WD-40 Domain Repeat of EML5 Leads to Decreased Bovine Sperm Quality and Fertility.

Authors:  Eriklis Nogueira; Filip Tirpák; Lauren E Hamilton; Michal Zigo; Karl Kerns; Miriam Sutovsky; JaeWoo Kim; Dietrich Volkmann; Luca Jovine; Jeremy F Taylor; Robert D Schnabel; Peter Sutovsky
Journal:  Front Cell Dev Biol       Date:  2022-04-05

4.  Loss of dystrophin and the microtubule-binding protein ELP-1 causes progressive paralysis and death of adult C. elegans.

Authors:  Jennifer L Hueston; Kathy A Suprenant
Journal:  Dev Dyn       Date:  2009-08       Impact factor: 3.780

5.  A doublecortin containing microtubule-associated protein is implicated in mechanotransduction in Drosophila sensory cilia.

Authors:  S Bechstedt; J T Albert; D P Kreil; T Müller-Reichert; M C Göpfert; J Howard
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Review 6.  Molecular mechanisms that underpin EML4-ALK driven cancers and their response to targeted drugs.

Authors:  Richard Bayliss; Jene Choi; Dean A Fennell; Andrew M Fry; Mark W Richards
Journal:  Cell Mol Life Sci       Date:  2016-01-11       Impact factor: 9.261

Review 7.  EML4-ALK Variants: Biological and Molecular Properties, and the Implications for Patients.

Authors:  Sarah R Sabir; Sharon Yeoh; George Jackson; Richard Bayliss
Journal:  Cancers (Basel)       Date:  2017-09-05       Impact factor: 6.639

8.  The C. elegans EMAP-like protein, ELP-1 is required for touch sensation and associates with microtubules and adhesion complexes.

Authors:  Jennifer L Hueston; Gina Purinton Herren; Juan G Cueva; Matthew Buechner; Erik A Lundquist; Miriam B Goodman; Kathy A Suprenant
Journal:  BMC Dev Biol       Date:  2008-11-17       Impact factor: 1.978

9.  Crystal structure of EML1 reveals the basis for Hsp90 dependence of oncogenic EML4-ALK by disruption of an atypical β-propeller domain.

Authors:  Mark W Richards; Edward W P Law; La'Verne P Rennalls; Sara Busacca; Laura O'Regan; Andrew M Fry; Dean A Fennell; Richard Bayliss
Journal:  Proc Natl Acad Sci U S A       Date:  2014-03-24       Impact factor: 11.205

  9 in total

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