Ono T, Okada S
Mutat Res. 1977 Apr;43(1):25-36. doi: 10.1016/0027-5107(77)90128-2.
Gamma-ray-induced DNA single-strand scissions and the ability to repair the scissions in spermatogonia from young mice and in spermatozoa from adult mice were studied quantitatively by an alkaline sucrose density-gradient centrifugation method. The average size of DNAs in non-irradiated spermatogonia was 2.6--3.0 X 10(8) daltons, similar to those of a spermatid-rich population, and the size of DNA in non-irradiated spermatozoa was 1.2 X 10(8) daltons. In spermatogonia, the radiosensitivity of DNA was 0.42 single-strand breaks/10(12) daltons of DNA/rad in oxic conditions and only 0.24 under anoxic conditions. In spermatozoa the break efficiency of DNA was 0.22 single-strand breaks/10(12) daltons of DNA/rad under oxic conditions and altered little under anoxic irradiation. The DNA scissions were efficiently repaired in spermatogonia within 10 min, whereas the breaks in spermatozoa were not rejoined at all even after two days of post-irradiation time. The radiosensitivities of DNA, repair capability and non- and/or slow-reparable DNA scissions were compared in spermatogonium-rich, spermatid-rich and spermatozoan-rich populations.
采用碱性蔗糖密度梯度离心法,对γ射线诱导的幼年小鼠精原细胞和成年小鼠精子中的DNA单链断裂及修复这些断裂的能力进行了定量研究。未受照射的精原细胞中DNA的平均大小为2.6 - 3.0×10⁸道尔顿,与富含精子细胞的群体相似,未受照射的精子中DNA的大小为1.2×10⁸道尔顿。在精原细胞中,有氧条件下DNA的放射敏感性为0.42条单链断裂/10¹²道尔顿DNA/拉德,而在无氧条件下仅为0.24。在精子中,有氧条件下DNA的断裂效率为0.22条单链断裂/10¹²道尔顿DNA/拉德,无氧照射下变化不大。精原细胞中的DNA断裂在10分钟内得到有效修复,而精子中的断裂即使在照射后两天也根本没有重新连接。对富含精原细胞、富含精子细胞和富含精子的群体中的DNA放射敏感性、修复能力以及不可修复和/或缓慢修复的DNA断裂进行了比较。