Literature DB >> 560258

The dynamics of maternal poly(A)-containing mRNA in fertilized sea urchin eggs.

F H Wilt.   

Abstract

Cytoplasmic polyadenylated RNA with the characteristics of sequestered mRNA exists in the unfertilized sea urchin egg. Following egg activation, the amount of poly(A) doubles, but total RNA content stays constant. Chromatography of the RNA on poly(U)-Sepharose shows that the amount of RNA that bears a poly(A) tract increases slightly (approximately 20-30%) during the 2 hr after fertilization. When a cDNA transcript of the poly(A)+ mRNA from 2 hr zygotes is reacted against poly(A)+ RNA from either eggs or zygotes, the kinetics of reassociation of the two preparations seem identical; hence the RNA sequences bearing poly(A) are the same in eggs and zygotes. Measurement of the length of the poly(A) tract in eggs and zygotes shows an increase in number average length from about 45 bases to 60 bases. Measurement of tract length of poly(A) in two cell zygotes by adenosine/AMP ratios of radioactive RNA shows that the poly(A) tract of the zygote is solely accounted for radioactive RNA, indicating extensive turnover of the poly(A). It is concluded that the poly(A) tract in these cells is subject to both lengthening and shortening, with the former predominating in this instance. the increase in poly(A) does not involve polyadenylation of different sequences, but is due to an increase in the number of polyadenylated sequences and the length of the poly(A) tracts that they bear.

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Year:  1977        PMID: 560258     DOI: 10.1016/0092-8674(77)90084-8

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


  20 in total

1.  Determination of the length distribution of poly(A) at the 3' terminus of the virion RNAs of EMC virus, poliovirus, rhinovirus, RAV-61 and CPMV and of mouse globin mRNA.

Authors:  P Ahlquist; P Kaesberg
Journal:  Nucleic Acids Res       Date:  1979-11-10       Impact factor: 16.971

2.  Ribonucleic Acid and protein metabolism in pea epicotyls : I. The aging process.

Authors:  A M Schuster; E Davies
Journal:  Plant Physiol       Date:  1983-11       Impact factor: 8.340

3.  A database of mRNA expression patterns for the sea urchin embryo.

Authors:  Zheng Wei; Robert C Angerer; Lynne M Angerer
Journal:  Dev Biol       Date:  2006-08-22       Impact factor: 3.582

4.  Storage of embryonically transcribed poly(A) RNA and its utilization during metamorphosis of the hydroidHydractinia echinata.

Authors:  Rolf Eiben
Journal:  Wilehm Roux Arch Dev Biol       Date:  1982-07

5.  Electron microscope visualization of giant polysomes in sea urchin embryos.

Authors:  Arthur H Whiteley; Shigeki Mizuno
Journal:  Wilehm Roux Arch Dev Biol       Date:  1981-03

6.  Cat-2 gene expression. Developmental control of translatable CAT-2 mRNA levels in maize scutellum.

Authors:  C C Kopczynski; J G Scandalios
Journal:  Mol Gen Genet       Date:  1986-04

7.  Molecular structure of maternal RNA.

Authors:  T L Thomas; J W Posakony; D M Anderson; R J Britten; E H Davidson
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

8.  Messenger RNA prevalence in sea urchin embryos measured with cloned cDNAs.

Authors:  L A Lasky; Z Lev; J H Xin; R J Britten; E H Davidson
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

9.  Induction of rat liver metallothionein mRNA and its distribution between free and membrane-bound polyribosomes.

Authors:  S G Shapiro; R J Cousins
Journal:  Biochem J       Date:  1980-09-15       Impact factor: 3.857

10.  Detection of poly A+ RNA in sea urchin eggs and embryos by quantitative in situ hybridization.

Authors:  L M Angerer; R C Angerer
Journal:  Nucleic Acids Res       Date:  1981-06-25       Impact factor: 16.971

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