Whitney J B, Mills T M, Lewis R W, Wartell R, Abney T O
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta 30912, USA.
Biochem Genet. 2000 Jun;38(5-6):119-37. doi: 10.1023/a:1001935012134.
Sex determination in the mammalian embryo begins with the activation of a gene on the Y chromosome which triggers a cascade of events that lead to male development. The mechanism by which this gene, designated SRY in humans and Sry in mice (sex determining region of the Y chromosome), is activated remains unknown. Likewise, the downstream target genes for Sry remain unidentified at present. C57BL mice carrying a Y chromosome from Mus musculus musculus or molossinus develop normally as males. In contrast, C57BL/6 mice with the Y chromosome from M. m. domesticus often show sex reversal, i.e., develop as XY females. It has been documented that C57BL mice with the Y chromosome from Poschiavinus (YPOS), a domesticus subtype, always develop as females or hermaphrodites. This suggests that a C57BL gene either up- or downstream of Sry is ineffective in interacting with Sry, which then compromises the processes that lead to normal male sex development. Nonetheless, by selective breeding, we have been able to generate a sex reversal-resistant C57BL/6-congenic strain of mice in which the XYPOS individuals consistently develop as normal males with bilateral testes. Because the resistance to sex reversal was transferred from strain 129S1/Sv (nonalbino) by simple selection over 13 backcross generations, it is inferred that a single autosomal gene or chromosomal region confers resistance to the sex reversal that would otherwise result. XYPOS normal males generated in these crosses were compared to XYPOS abnormal individuals and to C57BL/6 controls for sexual phenotype, gonadal weight, serum testosterone, and major urinary protein (MUP) level. A clear correlation was found among phenotypic sex, MUP level, and testis weight in the males and in the incompletely masculinized XYPOS mice. The fully masculinized males of the congenic strain resemble C57BL/6 males in the tested parameters. DNA analysis confirmed that these males, in fact, carry the YPOS Sry gene.
哺乳动物胚胎中的性别决定始于Y染色体上一个基因的激活,该基因引发一系列导致雄性发育的事件。这个在人类中被称为SRY、在小鼠中被称为Sry(Y染色体性别决定区域)的基因被激活的机制仍然未知。同样,目前Sry的下游靶基因也尚未确定。携带小家鼠或小家鼠穆氏亚种Y染色体的C57BL小鼠通常发育为正常雄性。相比之下,携带小家鼠家鼠亚种Y染色体的C57BL/6小鼠经常出现性反转,即发育为XY雌性。据记载,携带波氏小家鼠(YPOS,家鼠亚种的一种)Y染色体的C57BL小鼠总是发育为雌性或雌雄同体。这表明,Sry上游或下游的一个C57BL基因在与Sry相互作用时无效,进而损害了导致正常雄性性别发育的过程。尽管如此,通过选择性育种,我们已经能够培育出一种抗性反转的C57BL/6同源近交系小鼠,其中XYPOS个体始终发育为具有双侧睾丸的正常雄性。由于通过13代回交的简单选择,性反转抗性从129S1/Sv(非白化)品系转移而来,因此推断单个常染色体基因或染色体区域赋予了对否则会发生的性反转的抗性。将这些杂交产生的XYPOS正常雄性与XYPOS异常个体以及C57BL/6对照进行性表型、性腺重量、血清睾酮和主要尿蛋白(MUP)水平的比较。在雄性和不完全雄性化的XYPOS小鼠中,表型性别、MUP水平和睾丸重量之间发现了明显的相关性。同源近交系的完全雄性化雄性在测试参数上类似于C57BL/6雄性。DNA分析证实,这些雄性实际上携带YPOS Sry基因。