DEVELOPMENTAL-CHANGES IN LEVELS OF PROOPIOMELANOCORTIN INTRON A-CONTAINING HETEROGENEOUS NUCLEAR-RNA AND MATURE MESSENGER-RNA IN THE ANTERIOR AND NEUROINTERMEDIATE LOBES OF THE RAT PITUITARY

被引:11
作者
SCOTT, REM
AUTELITANO, DJ
LUGO, DI
BLUM, M
ROBERTS, JL
PINTAR, JE
机构
[1] COLUMBIA UNIV COLL PHYS & SURG, DEPT ANAT & CELL BIOL, 630 W 168 ST, NEW YORK, NY 10032 USA
[2] MT SINAI MED SCH, FISHBERG CTR NEUROBIOL, NEW YORK, NY 10027 USA
关键词
D O I
10.1210/mend-4-6-812
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The POMC cells of the rat pituitary undergo dynamic phenotypic changes during differentiation. Here we have determined that alterations in the relative levels of a POMC precursor RNA species and POMC mRNA occur during development and may represent another level at which the POMC phenotype is developmentally regulated. We performed solution hy-bridization/nuclease protection assays using a POMC exon 1/intron A splice junction probe to quantitate levels of both intron A-containing POMC heterogeneous nuclear (hnRNA) and fully processed POMC mRNA in separated anterior and neurointermediate lobes of the fetal, neonatal, and adult pituitary. The levels of POMC hnRNA per anterior lobe increased 7-fold from embryonic day 15 to adulthood (0.022 to 0.159 fmol/lobe), while POMC mRNA levels increased 121-fold (0.15 to 18.2 fmol/lobe). POMC hnRNA levels per neurointermediate lobe increased 23-fold from embryonic day 18 to adulthood (0.024 to 0.54 fmol/lobe), while POMC mRNA levels increased 69-fold (0.65 to 44.6 fmol/lobe). Thus, both anterior and neurointermediate lobes contain higher relative abundances of POMC hnRNA compared to mRNA during early development. These subsequently decrease (from 1:7 to 1:~110 in the anterior lobe and from 1:27 to 1:83 in the intermediate lobe over the ages examined) as the levels of POMC mRNA in both anterior and neurointermediate lobe increase at a greater rate than POMC hnRNA as development progresses. These results provide the first measurements of POMC mRNA and hnRNA levels during ontogeny and suggest that there may be a developmental change in the regulation of POMC primary transcript processing. © 1990 by The Endocrine Society.
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页码:812 / 820
页数:9
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