Micropropagation by tissue culture triggers differential expression of infectious endogenous Banana streak virus sequences (eBSV) present in the B genome of natural and synthetic interspecific banana plantains

The genome of Musa balbisiana spp. contains several infectious endogenous sequences of Banana streak virus (eBSV). We have shown previously that in vitro micropropagation triggers the activation of infectious eBSOLV (endogenous sequences of Banana streak Obino l'Ewai virus ) in the synthetic tetraploid interspecific hybrid FHIA21 (AAAB). In this work, we show that another synthetic tetraploid (AAAB) hybrid and two natural triploid (AAB) plantains are equally prone to the activation of infectious eBSOLV during tissue culture. These results are a strong indication that such activation is a general phenomenon in interspecific Musa cultivars, whether synthetic or natural. We also report the first in-depth study of the correlation between the duration of tissue culture and the level of activation of infectious eBSOLV, and show that specific and common activation patterns exist in these banana plants. We hypothesize that these patterns result from the concomitant activation of infectious eBSOLV and a decrease in the virus titre in neoformed plantlets, resulting from cell multiplication outcompeting virus replication. We provide experimental data supporting this hypothesis. No activation of infectious eBSGFV (endogenous sequences of Banana streak Goldfinger virus) by tissue culture was observed in the two natural AAB plantain cultivars studied here, whereas such activation occurred in the AAAB synthetic hybrid studied. We demonstrate that this differential activation does not result from differences in the structure of eBSGFV, as all banana genomes harbour eaBSGFV-7.     

Cyclic Expression of A Nuclear Protein In A Dinoflagellate

Nuclei of the dinoflagellate Crypthecodinium cohnii strain Whd were isolated and nuclear proteins were extracted in three fractions, corresponding to the increasing affinity of these proteins to genomic DNA. One fraction contained two major bands (48- and 46-kDa) and antibodies specific to this fraction revealed two major bands by Western blot on nuclear extracts, corresponding to the 46- and 48-kDa bands. The 48-kDa protein was detected in G1 phase but not in M phase cells. An expression cDNA library of C. cohnii was screened with these antibodies, and two different open reading frames were isolated. Dinoflagellate nuclear associated protein (Dinap1), one of these coding sequences, was produced in E. coli and appeared to correspond to the 48-kDa nuclear protein. No homologue of this sequence was found in the data bases, but two regions were identified, one including two putative zinc finger repeats, and one coding for two potential W/W domains. The second coding sequence showed a low similarity to non-specific sterol carrier proteins. Immunocytolocalization with specific polyclonal antibodies to recombinant Dinap1 showed that the nucleus was immunoreactive only during the G1 phase: the nucleoplasm was immunostained, while chromosome cores and nuclear envelopes were negative.     

Swimming medusoid gonophores in two species of Sertularella (Cnidaria,Hydrozoa, Sertulariidae) from Réunion Island,Indian Ocean

Summary

Two life cycle patterns predominate in thecate hydroids, those with alternating polyp and medusa stages, and those with fixed gonophores. Relatively few species release short-lived medusoids, also called swimming gonophores, that carry the gametes. In the family Sertulariidae, with its large number of taxa, this mode of metagenesis has been documented previously for only two species. It is described here for two others, Sertularella diaphana (Allman, 1885) and Sertularella n. sp., from the coastal waters of Reunion Island. Freshly collected fertile male and female colonies released medusoids near dawn, one per gonotheca. Strong contractions of the bell in the swimming movements induced the shedding of gametes. Once gametes were shed, medusoids quickly degenerated and died. The medusoids were similar morphologically in these two related species, and no obvious sexual dimorphism was noted. They were ovoid in shape, the spadix was eccentric, and a velum was present; but they lacked a mouth, tentacles, sense organs, and radial and circular canals as described earlier in Amphisbetia operculata (Linneus, 1758) and Sertularia marginata Kirchenpauer, 1864. However, the medusoids described here lacked exumbrellar nematocysts. Moreover, the spadix with its dense mass of gametes was different from all other described in being stuck from base to top on one side of the subumbrella in spite of hanging freely in the subumbrellar cavity. The hypothesis that this unusual reproductive mode in sertulariids has been underestimated is confirmed by these findings.