Literature DB >> 7352033

Histone H5 messenger RNA is polyadenylated.

H V Molgaard, M Perucho, A Ruiz-Carrillo.   

Abstract

In most known systems, histone mRNA lacks the poly(A) sequence at the 3' end of the molecule typical of most mRNAs. Furthermore, the synthesis of histones, unlike that of most proteins, is tightly coupled to DNA synthesis. Nevertheless, histone synthesis occurs in amphibian oocytes in the absence of DNA synthesis. Moreover, it has recently been found that in amphibian oocytes most of the histone mRNA is polyadenylated, and the polyadenylate is probably removed during maturation of the oocyte. Histone H5, an H1-like tissue-specific histone occurring only in nucleated erythrocytes, is also atypical in that it is synthesised in the absence of DNA synthesis during maturation of the red blood cells. We report here that H5 mRNA is polyadenylated.

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Year:  1980        PMID: 7352033     DOI: 10.1038/283502a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  16 in total

1.  Regulation of histone and beta A-globin gene expression during differentiation of chicken erythroid cells.

Authors:  M Affolter; J Côté; J Renaud; A Ruiz-Carrillo
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

2.  Different 3'-end processing produces two independently regulated mRNAs from a single H1 histone gene.

Authors:  G H Cheng; A Nandi; S Clerk; A I Skoultchi
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

3.  Butyrate induced accumulation of a 2.3 kb polyadenylated H1(0) histone mRNA in HeLa cells.

Authors:  H Kress; R Tönjes; D Doenecke
Journal:  Nucleic Acids Res       Date:  1986-09-25       Impact factor: 16.971

4.  Transcription of the chicken histone H5 gene is mediated by distinct tissue-specific elements within the promoter and the 3' enhancer.

Authors:  C D Trainor; J D Engel
Journal:  Mol Cell Biol       Date:  1989-05       Impact factor: 4.272

5.  The stem-loop structure at the 3' end of histone mRNA is necessary and sufficient for regulation of histone mRNA stability.

Authors:  N B Pandey; W F Marzluff
Journal:  Mol Cell Biol       Date:  1987-12       Impact factor: 4.272

6.  Histone mRNA degradation in vivo: the first detectable step occurs at or near the 3' terminus.

Authors:  J Ross; S W Peltz; G Kobs; G Brewer
Journal:  Mol Cell Biol       Date:  1986-12       Impact factor: 4.272

7.  The histone H5 gene is flanked by S1 hypersensitive structures.

Authors:  A Ruiz-Carrillo
Journal:  Nucleic Acids Res       Date:  1984-08-24       Impact factor: 16.971

8.  The histone H3 and H4 mRNAs are polyadenylated in maize.

Authors:  N Chaubet; M E Chaboute; B Clément; M Ehling; G Philipps; C Gigot
Journal:  Nucleic Acids Res       Date:  1988-02-25       Impact factor: 16.971

9.  Replacement variant histone genes contain intervening sequences.

Authors:  D Brush; J B Dodgson; O R Choi; P W Stevens; J D Engel
Journal:  Mol Cell Biol       Date:  1985-06       Impact factor: 4.272

10.  Chicken histone H5 mRNA: the polyadenylated RNA lacks the conserved histone 3' terminator sequence.

Authors:  P A Krieg; A J Robins; A Colman; J R Wells
Journal:  Nucleic Acids Res       Date:  1982-11-11       Impact factor: 16.971

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