Suda Mari, Uno Yoshinobu, Mori Yumiko, Matsuda Yoichi, Nakamura Masahisa
Department of Biology, Faculty of Education and Integrated Arts and Sciences, Waseda University, Tokyo, Japan.
J Exp Zool A Ecol Genet Physiol. 2011 Apr 1;315(4):222-31. doi: 10.1002/jez.668. Epub 2011 Feb 16.
We performed a molecular cloning of the glutamic oxaloacetic transaminase (GOT1) gene from R. rugosa, and determined its chromosomal location. This gene was reportedly localized near the sex-determining region of the ZW sex chromosomes in the frog Buergeria buergeri; however, the GOT1 gene was mapped to the distal end of chromosome 9 in R. rugosa using a GOT1 cDNA FISH probe. This was also the case when a 46.3 kb genomic clone containing exon 8 and 9 and the 3'-neighboring region of the GOT1 gene, designated clone B, was used as probe. However, weak signals were also detected at the telomeric ends of other autosomes and the Z sex chromosome, and near the centromeric region of the W sex chromosome. To intensify the signals, we used eight internal fragments in clone B and applied them to chromosome mapping. Consequently, only two fragments containing repeated sequence blocks produced hybridization signals; those signals were observed on autosomes and ZW sex chromosomes. The 3'-neighboring region contained two types of repeated sequence elements: a 41 bp element, designated 41-REL, localized to telomeric ends of autosomes and a 31 bp element, designated 31-REL, localized to telomeric ends of all autosomes and the ZW sex chromosomes, and also near the centromere on the W long arm. The results collectively suggest that the two repeated sequence elements were independently amplified around the chromosomal telomeres in R. rugosa, indicating that they will be useful cytogenetic markers for studying karyotypic evolution-especially the W chromosome differentiation-in this species.
我们对玫瑰(R. rugosa)的谷氨酸草酰乙酸转氨酶(GOT1)基因进行了分子克隆,并确定了其染色体定位。据报道,该基因位于蛙类日本林蛙(Buergeria buergeri)ZW性染色体的性别决定区域附近;然而,使用GOT1 cDNA FISH探针将GOT1基因定位到了玫瑰的9号染色体远端。当使用包含外显子8和9以及GOT1基因3'侧翼区域的46.3 kb基因组克隆(命名为克隆B)作为探针时,情况也是如此。然而,在其他常染色体和Z性染色体的端粒末端以及W性染色体的着丝粒区域附近也检测到了微弱信号。为了增强信号,我们在克隆B中使用了八个内部片段并将它们应用于染色体定位。结果,只有两个包含重复序列块的片段产生了杂交信号;这些信号在常染色体和ZW性染色体上均有观察到。3'侧翼区域包含两种类型的重复序列元件:一种41 bp的元件,命名为41-REL,定位于常染色体的端粒末端;另一种31 bp的元件,命名为31-REL,定位于所有常染色体和ZW性染色体的端粒末端,以及W长臂的着丝粒附近。这些结果共同表明,这两种重复序列元件在玫瑰的染色体端粒周围独立扩增,表明它们将成为研究该物种核型进化——尤其是W染色体分化——的有用细胞遗传学标记。