Literature DB >> 1808207

Ectopic expression of an A-type lamin does not interfere with differentiation of lamin A-negative embryonal carcinoma cells.

M Peter1, E A Nigg.   

Abstract

The nuclear lamina is an intermediate filament-type network underlying the inner nuclear membrane. It is believed to be important for nuclear envelope integrity and the organization of interphase chromatin. On the basis of biochemical properties and sequence criteria, vertebrate lamin proteins are classified as either A- or B-type. While B-type lamins are expressed in almost all cell types, no A-type lamins are present in early vertebrate embryos or undifferentiated embryonal carcinoma cell lines. Intriguingly, expression of A-type lamins occurs concomitant with cell differentiation and embryonic development. These findings have led to the hypothesis that A-type lamins might play a role in establishing or stabilizing cell-type specific differences in nuclear organization, which in turn might relate to the developmental potential of a cell. To test this hypothesis, we have stably expressed chicken lamin A in undifferentiated murine embryonal carcinoma (P19) cells, and examined the consequences of ectopic lamin A expression for the differentiation state and potential of these cells. Our results demonstrate that the P19 cells, although normally devoid of lamin A, properly incorporate and process chicken lamin A. Moreover, the stably transfected cell lines maintain the properties of undifferentiated cells, demonstrating that expression of lamin A does not directly induce differentiation. Conversely, when exposed to retinoic acid, an inducer of differentiation, lamin A-expressing P19 cells are able to differentiate normally. Taken together, our results suggest that unscheduled expression of A-type lamins is not sufficient to deregulate cell differentiation programs. The implications of these findings for the possible role for lamin A expression during development are discussed.

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Year:  1991        PMID: 1808207     DOI: 10.1242/jcs.100.3.589

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  8 in total

1.  Increased expression of Syne1/nesprin-1 facilitates nuclear envelope structure changes in embryonic stem cell differentiation.

Authors:  Elizabeth R Smith; Xiao-Ying Zhang; Callinice D Capo-Chichi; Xiongwen Chen; Xiang-Xi Xu
Journal:  Dev Dyn       Date:  2011-08-23       Impact factor: 3.780

2.  Lamin C and chromatin organization in Drosophila.

Authors:  B V Gurudatta; L S Shashidhara; Veena K Parnaik
Journal:  J Genet       Date:  2010-04       Impact factor: 1.166

3.  Post-natal myogenic and adipogenic developmental: defects and metabolic impairment upon loss of A-type lamins.

Authors:  Nard Kubben; Jan Willem Voncken; Gonda Konings; Michel van Weeghel; Maarten Mg van den Hoogenhof; Marion Gijbels; Arie van Erk; Kees Schoonderwoerd; Bianca van den Bosch; Vivian Dahlmans; Chantal Calis; Sander M Houten; Tom Misteli; Yigal M Pinto
Journal:  Nucleus       Date:  2011 May-Jun       Impact factor: 4.197

4.  Thyroid hormone-regulated expression of nuclear lamins correlates with dedifferentiation of intestinal epithelial cells during Xenopus laevis metamorphosis.

Authors:  Takashi Hasebe; Mitsuko Kajita; Mari Iwabuchi; Keita Ohsumi; Atsuko Ishizuya-Oka
Journal:  Dev Genes Evol       Date:  2011-08-25       Impact factor: 0.900

5.  The gene structure of Xenopus nuclear lamin A: a model for the evolution of A-type from B-type lamins by exon shuffling.

Authors:  R Stick
Journal:  Chromosoma       Date:  1992-08       Impact factor: 4.316

6.  Phosphorylation on protein kinase C sites inhibits nuclear import of lamin B2.

Authors:  H Hennekes; M Peter; K Weber; E A Nigg
Journal:  J Cell Biol       Date:  1993-03       Impact factor: 10.539

Review 7.  Building up the nucleus: nuclear organization in the establishment of totipotency and pluripotency during mammalian development.

Authors:  Máté Borsos; Maria-Elena Torres-Padilla
Journal:  Genes Dev       Date:  2016-03-15       Impact factor: 11.361

8.  SSEA3 and Sialyl Lewis a Glycan Expression Is Controlled by B3GALT5 LTR through Lamin A-NFYA and SIRT1-STAT3 Signaling in Human ES Cells.

Authors:  Bi-He Cai; Hsueh-Yi Lee; Chi-Kan Chou; Po-Han Wu; Hsiang-Chi Huang; Chia-Chun Chao; Hsiao-Yu Chung; Reiji Kannagi
Journal:  Cells       Date:  2020-01-10       Impact factor: 6.600

  8 in total

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