The Drosophila melanogaster "always early" gene (Dmaly)， which is required for G2/M cell-cycle control and spermatid differentiation， is one of the meiotic arrest genes. To study the Bombyx mori aly gene (Bmaly)， the cDNA of Bmaly was cloned and sequenced， and the results showed that the open reading frame of Bmaly is 1，713 bp in length， encoding 570 amino acid residues， in which a domain in an Rb-related pathway was found. Phylogenetic analysis based on the amino acid sequence of conserved regions showed that Aly from different insects gathered together， except for DmAly and Culex quinquefasciatus Aly， which were not clustered to a subgroup according to insect order. The Bmaly gene was insert... More
The Drosophila melanogaster "always early" gene (Dmaly)， which is required for G2/M cell-cycle control and spermatid differentiation， is one of the meiotic arrest genes. To study the Bombyx mori aly gene (Bmaly)， the cDNA of Bmaly was cloned and sequenced， and the results showed that the open reading frame of Bmaly is 1，713 bp in length， encoding 570 amino acid residues， in which a domain in an Rb-related pathway was found. Phylogenetic analysis based on the amino acid sequence of conserved regions showed that Aly from different insects gathered together， except for DmAly and Culex quinquefasciatus Aly， which were not clustered to a subgroup according to insect order. The Bmaly gene was inserted into expression vector pGS-21a(+) and then the recombinant protein was expressed in Escherichia coli and used to immunize mice to prepare the antibody against BmAly. Immunofluorescence examination showed that BmAly was distributed in both the cytoplasm and nucleus of BmN cell. The Bmaly gene expression could not be detected in the silk gland， malpighian tubule， fat body， or midgut of the silkworm. Expression levels of the Bmaly gene were detected in the gonadal tissues， where the levels in the testes were 10 times higher than that in the ovaries. Moreover， Bmaly expression was detected by quantitative polymerase chain reaction at different stages of B. mori testis development， at which fifth instar was relatively grossly expressed. The result suggested Bmaly was abundantly expressed in primary spermatocytes and prespermatids. To further explore the function of Bmaly， Bmaly siRNA was injected into third and fourth instar silkworm larvae， which markedly inhibited the development of sperm cells. These results together suggest that Bmaly is a meiotic arrest gene that plays an important role in spermatogenesis.
