Literature DB >> 987857

On the existence of polyadenylated histone mRNA in Xenopus laevis oocytes.

R G Levenson, K B Marcu.   

Abstract

In a variety of systems, histone mRNA has been shown to lack poly(A) (Adesnik and Darnell, 1972; Grunstein et al., 1973). We have found, however, that in Xenopus laevis oocytes, poly (A)-containing mRNA codes for histones, in a wheat germ cell-free system, based on the following criteria: first, co-migration with authentic X. laevis oocyte histones on polyacrylamide gels; second, no detectable incorporation of tryptophan; third, differential incorporation of lysine and methionine into histone fraction H2A; fourth, resistance of histone fraction H2A to cleavage with cyanogen bromide; and fifth, correspondence of tryptic peptide maps of partially purified cell-free products with authentic X. laevis oocyte histone. RNA which directs the synthesis of histones in the cell-free system is retained on oligo(dT)-cellulose, even after denaturation in 80% DMSO at 70 degrees C, thereby demonstrating the covalent attachment of polyadenylic acid sequences to the mRNA. Poly (A)- RNA (7S-14S fraction) was also found to code for histones using the same criteria. We discuss the significance of the finding that X. laevis oocytes contain two classes of histone mRNA as well as the potential developmental implications of this observation.

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Year:  1976        PMID: 987857     DOI: 10.1016/0092-8674(76)90121-5

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  18 in total

1.  The oligo(A) tail on histone mRNA plays an active role in translational silencing of histone mRNA during Xenopus oogenesis.

Authors:  Ricardo Sánchez; William F Marzluff
Journal:  Mol Cell Biol       Date:  2004-03       Impact factor: 4.272

2.  Two Xenopus proteins that bind the 3' end of histone mRNA: implications for translational control of histone synthesis during oogenesis.

Authors:  Z F Wang; T C Ingledue; Z Dominski; R Sanchez; W F Marzluff
Journal:  Mol Cell Biol       Date:  1999-01       Impact factor: 4.272

3.  Renaturation kinetics of cDNA complementary to cytoplamic polyadenylated RNA from rainbow trout testis. Accessibility of transcribed genes to pancreatic DNase.

Authors:  B Levy; G H Dixon
Journal:  Nucleic Acids Res       Date:  1977-04       Impact factor: 16.971

4.  Noncoincidence of histone and DNA synthesis in cleavage cycles of early development.

Authors:  R J Arceci; P R Gross
Journal:  Proc Natl Acad Sci U S A       Date:  1977-11       Impact factor: 11.205

5.  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

6.  Giant readthrough transcription units at the histone loci on lampbrush chromosomes of the newt Notophthalmus.

Authors:  M O Diaz; J G Gall
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

7.  A histone H1 protein in sea urchins is encoded by a poly(A)+ mRNA.

Authors:  T Lieber; L M Angerer; R C Angerer; G Childs
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

8.  A unique subspecies of histone H4 mRNA from rat myoblasts contains poly(A).

Authors:  R C Bird; F A Jacobs; G Stein; J Stein; B H Sells
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

9.  Reassessment of histone gene expression during cell cycle in human cells by using homologous H4 histone cDNA.

Authors:  S Detke; A Lichtler; I Phillips; J Stein; G Stein
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

10.  Characterization of histone genes isolated from Xenopus laevis and Xenopus tropicalis genomic libraries.

Authors:  I Ruberti; P Fragapane; P Pierandrei-Amaldi; E Beccari; F Amaldi; I Bozzoni
Journal:  Nucleic Acids Res       Date:  1982-12-11       Impact factor: 16.971

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