Literature DB >> 1782138

A Xenopus multifinger protein, Xfin, is expressed in specialized cell types and is localized in the cytoplasm.

S De Lucchini1, F M Rijli, G Ciliberto, G Barsacchi.   

Abstract

Xfin is a member of a large family of Krüppel-type transcripts stored in the Xenopus egg, whose function is unknown. By using polyclonal antibodies raised against fusion proteins containing different portions of Xfin, we have identified the Xfin gene product and established its pattern of expression in some adult tissues and during oogenesis and embryogenesis. The corresponding mRNA localization has been studied by in situ hybridization on ovary and testis sections. The Xfin product is found in the cytoplasm, both during oogenesis and adulthood; in adult tissues, it is differentially expressed in a cell-type specific fashion. The expression of the protein in specialized cell types and its cytoplasmic localization may favour the hypothesis that it could be involved in cell differentiation events through protein-RNA interactions.

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Year:  1991        PMID: 1782138     DOI: 10.1016/0925-4773(91)90069-i

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  4 in total

1.  RNA binding properties and evolutionary conservation of the Xenopus multifinger protein Xfin.

Authors:  M Andreazzoli; S De Lucchini; M Costa; G Barsacchi
Journal:  Nucleic Acids Res       Date:  1993-09-11       Impact factor: 16.971

Review 2.  Genetic control of development in Xenopus laevis.

Authors:  R Vignali; S De Lucchini; B Kablar; G Barsacchi
Journal:  Genetica       Date:  1994       Impact factor: 1.082

3.  Clustered organization of homologous KRAB zinc-finger genes with enhanced expression in human T lymphoid cells.

Authors:  E J Bellefroid; J C Marine; T Ried; P J Lecocq; M Rivière; C Amemiya; D A Poncelet; P G Coulie; P de Jong; C Szpirer
Journal:  EMBO J       Date:  1993-04       Impact factor: 11.598

4.  The B-subdomain of the Xenopus laevis XFIN KRAB-AB domain is responsible for its weaker transcriptional repressor activity compared to human ZNF10/Kox1.

Authors:  Nadine Born; Hans-Jürgen Thiesen; Peter Lorenz
Journal:  PLoS One       Date:  2014-02-03       Impact factor: 3.240

  4 in total

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