First intron excision of GnRH pre-mRNA during postnatal development of normal mice and adult hypogonadal mice

Jae Young Seong, Won Kim Bong Won Kim, S. Park, Hoon Son Gi Hoon Son, K. Kim

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Previously, we demonstrated that excision of the GnRH first intron (intron A) was largely attenuated in non-GnRH-producing tissues but accelerated in GnRH neurons. In the present study, we examined the splicing rate of GnRH prem-RNA in developing normal mice and adult hypogonadal mice. The preoptic area and cerebral cortex were removed from mice at ages 1-7 wk. GnRH pre-mRNA splicing was examined by competitive RT-PCR using a variety of primer sets. The ratio of mature mRNA to intron A-containing RNA species in the preoptic area was lowest in 1- and 2-wk-old mice, significantly augmented in 3-wk-old mice, and further increased until adulthood. In contrast, the ratio of mRNA to intron A-containing RNA in the cerebral cortex was extremely low, drastically decreased in 3-wk-old mice, and remained at low levels until adulthood. These data indicate a preoptic area-specific increase in intron A excision during development. Intron B or C excision in the preoptic area was not significantly changed during development. To elucidate the possible involvement of the exonic splicing enhancers located in GnRH exons 3 and 4 in the developmental increase in intron A excision, we examined the splicing rate of GnRH pre-mRNA in hypogonadal mice whose GnRH exons 3 and 4 were truncated. The intron A excision in the preoptic area of hypogonadal mice was significantly lower than that of normal mice but similar to that in other tissues, such as cerebral cortex and olfactory bulb. To support the functional relevance of intron A-containing RNA species, we examined the translation efficiency of intron A-containing RNA. Insertion of intron A sequence into the upstream portion of the luciferase open reading frame significantly decreased translation efficiency. The present study demonstrates that intron A excision in the pre-optic area is developmentally regulated in normal mice but largely attenuated in hypogonadal mice, indicating the functional importance of intron A excision in GnRH pre-mRNA splicing.

Original languageEnglish
Pages (from-to)4454-4461
Number of pages8
JournalEndocrinology
Volume142
Issue number10
DOIs
Publication statusPublished - 2001 Oct 9
Externally publishedYes

Fingerprint

RNA Precursors
Gonadotropin-Releasing Hormone
Introns
Preoptic Area
RNA
Cerebral Cortex
Exons
Messenger RNA
Olfactory Bulb
Luciferases
Open Reading Frames

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism

Cite this

First intron excision of GnRH pre-mRNA during postnatal development of normal mice and adult hypogonadal mice. / Seong, Jae Young; Bong Won Kim, Won Kim; Park, S.; Gi Hoon Son, Hoon Son; Kim, K.

In: Endocrinology, Vol. 142, No. 10, 09.10.2001, p. 4454-4461.

Research output: Contribution to journalArticle

Seong, Jae Young ; Bong Won Kim, Won Kim ; Park, S. ; Gi Hoon Son, Hoon Son ; Kim, K. / First intron excision of GnRH pre-mRNA during postnatal development of normal mice and adult hypogonadal mice. In: Endocrinology. 2001 ; Vol. 142, No. 10. pp. 4454-4461.
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