Sparkes R S, Mohandas T, Sparkes M C, Shulkin J D
Biochem Genet. 1978 Aug;16(7-8):751-6. doi: 10.1007/BF00484732.
Three separate somatic cell fusions were made between Chinese hamster lines and human lymphocytes containing (1) a 3/4 translocation, (2) an X/9 translocation, and (3) a 17/9 translocation. Eleven independently derived hybrids showed that only human chromosome 22 was consistently present when human ACONM was expressed and absent when human ACONM was not expressed. These studies assign a gene for human ACONM to chromosome 22, and are consistent with prior gene-mapping results.
在中国仓鼠细胞系与含有(1)3/4易位、(2)X/9易位和(3)17/9易位的人淋巴细胞之间进行了三次独立的体细胞融合。十一个独立衍生的杂种显示,当人ACONM表达时,只有人类22号染色体始终存在,而当人ACONM不表达时则不存在。这些研究将人ACONM基因定位到22号染色体上,并且与先前的基因定位结果一致。