Me. Percy et al., LOCALIZATION OF A NEW FERRITIN HEAVY-CHAIN SEQUENCE PRESENT IN HUMAN BRAIN MESSENGER-RNA TO CHROMOSOME-11, Genome, 38(3), 1995, pp. 450-457
Two types of ferritin heavy CH) chain clones have been isolated from c
DNA libraries of human fetal and adult brain: one corresponds to the f
erritin H chain mRNA that is abundant in liver and is called ''liver-l
ike'' brain cDNA; the other contains an additional 279 nucleotide (nt)
sequence in the 3'untranslated region and is called brain ferritin H
chain cDNA. To map the 279-nt sequence, polymerase chain reaction (PCR
) amplification was carried out using DNA from rodent X human hybrid c
ell lines containing single human chromosomes as templates, and oligom
eric primers homologous to the 3'end of the 279-nt sequence (primer A)
and to a coding sequence just 5' to the 279-nt sequence. Significant
PCR product of the size expected from analysis of the brain ferritin H
chain cDNA clones and a genomic ferritin H chain clone (487 bp) was g
enerated only from hybrid-cell DNA containing human chromosome 11. Thi
s PCR product and the ''liver-like'' brain cDNA (lacking the 279-nt se
quence) both hybridized to chromosome 11 fragments that are known to d
efine the well-characterized functional liver ferritin 11 chain gene a
nd a putative pseudogene. preliminary data indicate that primer A (and
thus the 279-nt sequence) maps to the functional ferritin H chain gen
e fragments, but binding to the pseudogene has not been ruled out.