Literature DB >> 2578115

Polyploid tissues in the nematode Caenorhabditis elegans.

E M Hedgecock, J G White.   

Abstract

During larval development, the number of somatic nuclei in C. elegans hermaphrodites increases from 558 to 959 (J. E. Sulston and H. R. Horvitz, Dev. Biol. 56, 110-156, 1977; J. E. Sulston et al., Dev. Biol. 100, 64-119, 1983). At the same time, the animals increase about 60-fold in volume. We have measured the DNA contents of several classes of nuclei by quantitating the fluorescence of Hoescht 33258 stained DNA (D. G. Albertson et al., Dev. Biol. 63, 165-178, 1978). Probably all embryonic nuclei, including those of neurons, muscles, hypodermis, and intestine, are diploid at hatching. Neurons, muscles, and nondividing hypodermal nuclei remain diploid throughout larval development. The DNA content of the intestinal nuclei doubles at the end of each larval stage, reaching 32C by the adult stage. New hypodermal cells, generated by division of seam cells in the larval stages, undergo an additional round of DNA replication before fusing with the major syncytium (hyp7, Sulston et al., 1983). Thus the larval hyp7 syncytium comprises a fixed number of diploid embryonic nuclei plus an increasing number of tetraploid postembryonic nuclei. Some of the endoreduplications that occur in the intestinal and hypodermal lineages of C. elegans may correspond to nuclear or cellular divisions in another nematode Panagrellus redivivus (P. W. Sternberg and H. R. Horvitz, Dev. Biol. 93, 181-205, 1982).

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Year:  1985        PMID: 2578115     DOI: 10.1016/0012-1606(85)90381-1

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


  75 in total

1.  Coordinates, DNA content and heterogeneity of cell nuclei and segments of the Caenorhabditis elegans intestine.

Authors:  Marc Wolf; Frank Nunes; Rüdiger J Paul
Journal:  Histochem Cell Biol       Date:  2005-11-03       Impact factor: 4.304

2.  Chromosomal clustering and GATA transcriptional regulation of intestine-expressed genes in C. elegans.

Authors:  Florencia Pauli; Yueyi Liu; Yoona A Kim; Pei-Jiun Chen; Stuart K Kim
Journal:  Development       Date:  2005-12-14       Impact factor: 6.868

3.  The cellular geometry of growth drives the amino acid economy of Caenorhabditis elegans.

Authors:  Jonathan Swire; Silke Fuchs; Jacob G Bundy; Armand M Leroi
Journal:  Proc Biol Sci       Date:  2009-05-13       Impact factor: 5.349

Review 4.  Endoreplication: polyploidy with purpose.

Authors:  Hyun O Lee; Jean M Davidson; Robert J Duronio
Journal:  Genes Dev       Date:  2009-11-01       Impact factor: 11.361

5.  mir-35 is involved in intestine cell G1/S transition and germ cell proliferation in C. elegans.

Authors:  Min Liu; Pengpeng Liu; Li Zhang; Qingchun Cai; Ge Gao; Wenxia Zhang; Zuoyan Zhu; Dong Liu; Qichang Fan
Journal:  Cell Res       Date:  2011-06-21       Impact factor: 25.617

6.  CDC-25.2, a C. elegans ortholog of cdc25, is essential for the progression of intestinal divisions.

Authors:  Yong-Uk Lee; Miseol Son; Jiyoung Kim; Yhong-Hee Shim; Ichiro Kawasaki
Journal:  Cell Cycle       Date:  2016       Impact factor: 4.534

Review 7.  Endoreplication and polyploidy: insights into development and disease.

Authors:  Donald T Fox; Robert J Duronio
Journal:  Development       Date:  2013-01-01       Impact factor: 6.868

Review 8.  The Caenorhabditis elegans epidermis as a model skin. I: development, patterning, and growth.

Authors:  Andrew D Chisholm; Tiffany I Hsiao
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2012-06-19       Impact factor: 5.814

9.  Spindle assembly checkpoint genes reveal distinct as well as overlapping expression that implicates MDF-2/Mad2 in postembryonic seam cell proliferation in Caenorhabditis elegans.

Authors:  Maja Tarailo-Graovac; Jun Wang; Jeffrey S C Chu; Domena Tu; David L Baillie; Nansheng Chen
Journal:  BMC Cell Biol       Date:  2010-09-21       Impact factor: 4.241

10.  Restricting dosage compensation complex binding to the X chromosomes by H2A.Z/HTZ-1.

Authors:  Emily L Petty; Karishma S Collette; Alysse J Cohen; Martha J Snyder; Györgyi Csankovszki
Journal:  PLoS Genet       Date:  2009-10-23       Impact factor: 5.917

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