Identification of the female-determining region of the W chromosome in Bombyxmori

The W chromosome of the silkworm Bombyx mori is devoid of functional genes, except for the putative female-determining gene ( Fem ). To localize Fem , we investigated the presence of W-specific DNA markers on strains in which an autosomal fragment containing dominant marker genes was attached to the...

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Veröffentlicht in:Genetica 2008, Vol.133 (3), p.269-282
Hauptverfasser: Abe, H., Fujii, T., Tanaka, N., Yokoyama, T., Kakehashi, H., Ajimura, M., Mita, K., Banno, Y., Yasukochi, Y., Oshiki, T., Nenoi, M., Ishikawa, T., Shimada, T.
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Sprache:eng
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Zusammenfassung:The W chromosome of the silkworm Bombyx mori is devoid of functional genes, except for the putative female-determining gene ( Fem ). To localize Fem , we investigated the presence of W-specific DNA markers on strains in which an autosomal fragment containing dominant marker genes was attached to the W chromosome. We produced new W-chromosomal fragments from the existing Zebra-W strain (T(W;3) Ze chromosome) by X-irradiation, and then carried out deletion mapping of these and sex-limited yellow cocoon strains (T(W;2) Y -Chu, -Abe and -Ban types) from different Japanese stock centers. Of 12 RAPD markers identified in the normal W chromosomes of most silkworm strains in Japan, the newly irradiated W(B-YL-YS) Ze chromosome contained three, the T(W;2) Y -Chu chromosome contained six, and the T(W;2) Y -Abe and -Ban chromosomes contained only one (W-Rikishi). To investigate the ability of the reduced W-chromosome translocation fragments to form heterochromatin bodies, which are found in nuclei of normal adult female sucking stomachs, we examined cells of the normal type p50 strain and the T(W;2) Y -Chu and -Abe strains. A single sex heterochromatin body was found in nuclei of p50 females, whereas we detected only small sex heterochromatin bodies in the T(W;2) Y -Chu strain and no sex heterochromatin body in the T(W;2) Y -Abe strain. Since adult females of all strains were normal and fertile, we conclude that only extremely limited region, containing the W-Rikishi RAPD sequence of the W chromosome, is required to determine femaleness. Based on a comparison of the normal W-chromosome and 7 translocation and W-deletion strains we present a map of Fem relative to the 12 W-specific RAPD markers.
ISSN:0016-6707
1573-6857
DOI:10.1007/s10709-007-9210-1