FUNCTIONAL DIFFERENCES BETWEEN ULTRABITHORAX PROTEIN ISOFORMS IN DROSOPHILA-MELANOGASTER - EVIDENCE FROM ELIMINATION, SUBSTITUTION AND ECTOPIC EXPRESSION OF SPECIFIC ISOFORMS
V. Subramaniam et al., FUNCTIONAL DIFFERENCES BETWEEN ULTRABITHORAX PROTEIN ISOFORMS IN DROSOPHILA-MELANOGASTER - EVIDENCE FROM ELIMINATION, SUBSTITUTION AND ECTOPIC EXPRESSION OF SPECIFIC ISOFORMS, Genetics, 136(3), 1994, pp. 979-991
The homeotic selector gene Ultrabithorax (Ubx) specifies regional iden
tities in multiple tissues within the thorax and abdomen of Drosophila
melanogaster. Ubx encodes a family of six developmentally specific ho
meodomain protein isoforms translated from alternatively spliced mRNAs
. The mutant allele Ubx(195) contains a stop codon in exon mil, one of
three differential elements, and consequently produces functional UBX
protein only from mRNAs of type IVa and IVb, which are expressed main
ly in the central nervous system. Although it retains activity for oth
er processes, Ubx(195) behaves like a null allele with respect to deve
lopment of the peripheral nervous system, indicating that UBX-IVa and
IVb alone do not contribute detectable Ubx function for this tissue. T
he mutant allele Ubx(MX17) contains an inversion of exon mII. We find
that this allele only produces mRNAs of type IVa, but the expression p
attern of the resulting UBX-IVa protein is indistinguishable from that
of total UBX protein expression in wild-type embryos. The phenotype o
f homozygous UbX(MX17) embryos indicates that UBX-IVa cannot substitut
e functionally for other isoforms to promote normal development of the
peripheral nervous system. This functional limitation is confirmed by
a detailed analysis of the peripheral nervous system in embryos that
express specific UBX isoforms ectopically under control of a heat shoc
k promoter. Additional observations suggest that UBX isoforms also dif
fer in their ability to function in other tissues.