Isolation and developmental expression of two nuclear receptors, MHR4 and beta FTZ-F1, in the tobacco hornworm, Manduca sexta

The cDNAs for two members of the nuclear receptor superfamily were isolated from the tobacco hornworm, Manduca sexta. The deduced amino acid sequence of MHR4 shows 93-95% identity in the DNA-binding domain and the first porti on of the hinge (D) region with the germ cell nuclear factor (GCNF)-related factors (GRFs) of the silkworm, Bombyx mori, and the mealworm, Tenebrio mo litor, and with a genomic sequence from the fruit fly, Drosophila melanogas ter. Northern blot hybridization showed that a 7.5 kb MHR4 mRNA appeared in Manduca abdominal epidermis just as the ecdysteroid titer began to decline during the larval molt, disappeared about 12 h later, then transiently rea ppeared shortly before larval ecdysis. During the pupal and adult molts, a similar pattern of expression was seen (the very end of the adult molt was not studied). At peak times of expression in the epidermis, MHR4 mRNA was a lso present in fat body and the central nervous system (CNS). The deduced a mino acid sequence of Manduca FTZ-F1 is 100% and 96% identical to that of B . mori and Drosophila beta FTZ-F1, respectively, in the DNA-binding domain and the adjacent hinge region including the FTZ-F1 box. Northern blot analy sis showed that the >9.5 kb beta FTZ-F1 mRNA appeared in Manduca epidermis during the decline of the ecdysteroid titer in the larval, pupal and adult molts as the first peak of MHR4 mRNA declined, then it disappeared in the l arval and pupal molts before the second peak of MHR4 appeared. beta FTZ-F1 mRNA was also found in fat body and the CNS at the time of peak expression in the epidermis during the larval and pupal molts. Both MHR4 and beta FTZ- F1 mRNAs were found in the testis during the onset of spermatogenesis in th e prepupal period. (C) 2001 Elsevier Science Ltd. All rights reserved.