Graduate School of Life Science, Hokkaido University, Kita 10 Nishi 8, Kita-ku, Sapporo, Hokkaido 060-0810, Japan.
Chromosome Res. 2011 Jul;19(5):635-44. doi: 10.1007/s10577-011-9223-6. Epub 2011 Jun 8.
Tokudaia osimensis (the Amami spiny rat) and Tokudaia tokunoshimensis (the Tokunoshima spiny rat) have a sex chromosome composition of XO/XO, no Y chromosome. The mammalian sex-determining gene, SRY, is also absent in these species, which indicates that these spiny rats exhibit a novel sex-determining mechanism that is independent of SRY. To identify a candidate gene that controls this mechanism, the copy numbers and chromosomal locations of 10 genes with important functions in gonadal differentiation were determined: ATRX, CBX2 (M33), DMRT1, FGF9, NR0B1 (DAX1), NR5A1 (Ad4BP/SF1), RSPO1, SOX9, WNT4, and WT1. Multiple bands were detected for NR0B1 in Southern blot analysis, which suggested the presence of multiple copies of the gene in the genomes of these two species. CBX2 was localized to two loci in both sexes of the two species by fluorescence in situ hybridization mapping: 3q24 and 6p11.2 in T. osimensis and 10q25-q26 and 14q12-q13.1 in T. tokunoshimensis. Quantification of copy numbers in the two species by quantitative real-time PCR indicated that there were two or three more copies of CBX2 per haploid genome in males (T. osimensis, n = 3; T. tokunoshimensis, n = 2) than in females (T. osimensis, n = 4; T. tokunoshimensis, n = 2), whereas NR0B1 was present as a single copy in both. The results suggest that additional copies of CBX2 in males might be involved in a novel sex-determining mechanism in species that lack SRY.
Tokudaia osimensis(奄美刺鼠)和 Tokudaia tokunoshimensis(德之岛刺鼠)的性染色体组成为 XO/XO,没有 Y 染色体。这些物种中也没有哺乳动物性别决定基因 SRY,这表明这些刺鼠表现出一种新的性别决定机制,与 SRY 无关。为了鉴定控制这种机制的候选基因,确定了 10 个在性腺分化中具有重要功能的基因的拷贝数和染色体位置:ATRX、CBX2(M33)、DMRT1、FGF9、NR0B1(DAX1)、NR5A1(Ad4BP/SF1)、RSPO1、SOX9、WNT4 和 WT1。Southern 印迹分析检测到 NR0B1 的多个条带,这表明该基因在这两个物种的基因组中存在多个拷贝。荧光原位杂交图谱将 CBX2 定位到两个物种的两个性别中的两个位置:T. osimensis 的 3q24 和 6p11.2 以及 T. tokunoshimensis 的 10q25-q26 和 14q12-q13.1。通过实时定量 PCR 对两个物种的拷贝数进行定量表明,雄性(T. osimensis,n = 3;T. tokunoshimensis,n = 2)比雌性(T. osimensis,n = 4;T. tokunoshimensis,n = 2)的每个单倍体基因组中多存在两个或三个 CBX2 拷贝,而 NR0B1 则仅存在一个拷贝。结果表明,雄性中 CBX2 的额外拷贝可能参与了缺乏 SRY 的物种的新性别决定机制。