Fujii T, Abe H, Kawamoto M, Banno Y, Shimada T
Graduate School of Bioresource and Bioenvironmental Science, Kyushu University, Fukuoka, Japan; Department of Agricultural and Environmental Biology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Insect Mol Biol. 2015 Apr;24(2):213-21. doi: 10.1111/imb.12150. Epub 2014 Dec 3.
The giant egg (Ge) locus is a Z-linked mutation that leads to the production of large eggs. Cytological observations suggest that an unusual translocation of a large fragment of the W chromosome bearing a putative egg size-determining gene, Esd, gave rise to giant egg mutants. However, there is currently no molecular evidence confirming either a W-Z translocation or the presence of Esd on the W chromosome. To elucidate the origin of giant egg mutants, we performed positional cloning. We observed that the Bombyx mori. orthologue of the human Phytanoyl-CoA dioxygenase domain containing 1 gene (PHYHD1) is disrupted in giant egg mutants. PHYHD1 is highly conserved in eukaryotes and is predicted to be a Fe(II) and 2-oxoglutarate-dependent oxygenase. Exon skipping in one of the two available Ge mutants is probably caused by the insertion of a non-long terminal repeat transposon into intron 4 in the vicinity of the 5' splice site. Segmental duplication in Ge(2) , an independent allele, was caused by unequal recombination between short interspersed elements inserted into introns 3 and 5. Our results indicate that (1) Bombyx PHYHD1 is responsible for the Ge mutants and that (2) the Ge locus is unrelated to the W-linked putative Esd. To our knowledge, this is the first report describing the phenotypic defects caused by mutations in PHYHD1 orthologues.
巨卵(Ge)基因座是一种Z连锁突变,会导致产生大型卵。细胞学观察表明,携带假定的卵大小决定基因Esd的W染色体大片段发生异常易位,从而产生了巨卵突变体。然而,目前尚无分子证据证实W-Z易位或W染色体上存在Esd。为了阐明巨卵突变体的起源,我们进行了定位克隆。我们观察到,家蚕中人类含植烷酰辅酶A双加氧酶结构域1基因(PHYHD1)的直系同源基因在巨卵突变体中被破坏。PHYHD1在真核生物中高度保守,预计是一种依赖铁(II)和2-氧代戊二酸的加氧酶。在两个可用的Ge突变体之一中,外显子跳跃可能是由于一个非长末端重复转座子插入到5'剪接位点附近的内含子4中所致。独立等位基因Ge(2)中的片段重复是由插入到内含子3和5中的短散在元件之间的不等交换引起的。我们的结果表明:(1)家蚕PHYHD1是导致Ge突变体的原因;(2)Ge基因座与W连锁的假定Esd无关。据我们所知,这是第一份描述由PHYHD1直系同源基因突变引起的表型缺陷的报告。