Expression of transcripts for human pro-melanin concentrating hormone
(pMCH) were studied in the hypothalamus, the primary location for pMCH
producing cells in the mammalian CNS. Human hypothalamic tissue was e
xtracted for total RNA and the cDNA generated with reverse transcripta
se (RT). PCR amplification with primers spanning exons 2 and 3 of the
pMCH human-variant genes (pMCHL), yielded an unspliced product, confir
ming prior work [T.B. Campbell, C.K. McDonald, M. Hagen, The effect of
structure in a long target RNA on ribozyme cleavage efficiency, Nucle
ic Acids Res. 25 (1997) 4985-4993]. In addition, this product was show
n to be exclusively antisense, and to be derived from the 5p (pMCHL1),
not the 5q (pMCHL2) locus. Thus, there is no evidence that the MCH pe
ptide-precursor molecule is produced in the brain by the human-variant
pMCHL loci. In contrast, corresponding RT-PCR for pMCH RNA generated
by the locus on 12q, demonstrated the presence of both sense and antis
ense spliced RNA. Partial sequencing of the spliced product confirmed
that production of at least the two C-terminal peptides would occur fr
om the 12q pMCH locus. The significance of the findings for pMCH and p
MCHL1 are discussed relative to what is known about the function of en
dogenous antisense RNA. (C) 1998 Published by Elsevier Science B.V. Al
rights reserved.