Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.1.30.1 (
S1 nuclease
)
3,660
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Fodrin (nonerythroid spectrin) and its associated proteins have been previously implicated in the establishment of specialized membrane-cytoskeletal domains in differentiating cells. Using antiserum which is monospecific for the alpha-subunit of fodrin, we demonstrate that
alpha-fodrin
is present in oocytes and adult tissues of Xenopus laevis. Analyses of the de novo synthesis of
alpha-fodrin
during embryonic development reveal that
alpha-fodrin
is synthesized in oocytes, but not during early development. To investigate the level of control of
alpha-fodrin
expression, we isolated two cDNA clones for oocyte
alpha-fodrin
. The oocyte cDNA clones were identified as encoding portions of
alpha-fodrin
based on DNA sequence analysis and on the comparison of the predicted amino acid sequence of the cDNAs with the known sequence of human erythrocyte alpha-spectrin. The Xenopus
alpha-fodrin
cDNAs hybridize to a transcript of approximately 9 kb on RNA blots, and probably to a single gene type on genomic DNA blots. Both RNA blot analyses and
S1 nuclease
protection assays with the Xenopus
alpha-fodrin
cDNAs demonstrate that the observed decline in the de novo synthesis of
alpha-fodrin
polypeptides is controlled by a dramatic decrease in the abundance of
alpha-fodrin
transcripts after fertilization. In contrast, levels of actin transcripts do not decrease during this period. Inasmuch as steady-state levels of
alpha-fodrin
transcripts rise by the neurula stage of development, these results suggest that the synthesis of
alpha-fodrin
polypeptides during embryonic development of Xenopus is regulated, rather than constitutive, and that the primary level of control is the steady-state abundance of mRNA.
...
PMID:Changes in the expression of alpha-fodrin during embryonic development of Xenopus laevis. 304 Jul 72