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吴培l林, 尹洪萍, 殷黎静, 朱 洁, 曾咏梅, 刘桂杰, 亢晓冬. 2009: Kit无义突变致W-3Bao小鼠生殖腺异常及纯合子贫血死亡. 动物学研究, 30(1): 45-52. DOI: 10.3724/SP.J.1141.2009.01045
引用本文: 吴培l林, 尹洪萍, 殷黎静, 朱 洁, 曾咏梅, 刘桂杰, 亢晓冬. 2009: Kit无义突变致W-3Bao小鼠生殖腺异常及纯合子贫血死亡. 动物学研究, 30(1): 45-52. DOI: 10.3724/SP.J.1141.2009.01045
WU Pei-lin, YIN Hong-ping, YIN Li-jing, ZHU Jie, ZENG Yong-mei, LIU Gui-jie, KANG Xiao. 2009. Gonadial Abnormality and Homozygous Decease from the Nonsense Mutation of Kit in W-3Bao Mouse. Zoological Research, 30(1): 45-52. DOI: 10.3724/SP.J.1141.2009.01045
Citation: WU Pei-lin, YIN Hong-ping, YIN Li-jing, ZHU Jie, ZENG Yong-mei, LIU Gui-jie, KANG Xiao. 2009. Gonadial Abnormality and Homozygous Decease from the Nonsense Mutation of Kit in W-3Bao Mouse. Zoological Research, 30(1): 45-52. DOI: 10.3724/SP.J.1141.2009.01045

Kit无义突变致W-3Bao小鼠生殖腺异常及纯合子贫血死亡

Gonadial Abnormality and Homozygous Decease from the Nonsense Mutation of Kit in W-3Bao Mouse

  • 摘要: W-3Bao是本研究组通过诱变获得、Kit无义突变的白斑小鼠。突变基因杂合子小鼠腹部、四肢肢端及尾尖白化,其部分精曲小管内无精原细胞。突变纯合子小鼠在胚胎后期色泽苍白、个体矮小,于出生前后死亡;血液学检查发现纯合子小鼠血色素极低且红细胞变大;18.5天胚胎的连续切片可见精曲小管轮廓欠清晰,精原细胞分散分布于睾丸间质,未迁入精曲小管;卵巢结构紊乱,无明显的原始卵泡结构;骨髓等器官组织未见显著异常。结论:Kit无义突变不仅导致了W-3Bao杂合子小鼠白斑形成及纯合子小鼠贫血死亡,同时影响生殖腺发育。

     

    Abstract: The W-3Bao mouse, which was obtained in previous ENU mutagenesis project, is a new mutant caused by the nonsense mutation of Kit gene. Mating and gross observing combining with PCR and sequencing were used for determining the genotypes of the W-3Bao mice. Embryonic development, hematological detection and histopathologic section methods were used for their phenotype analysis. The results showed that the W-3Bao/+ mouse was white belly, white limb terminals and white tail tip. However, there was no difference of the external appearance among the W-3Bao/+, W-3Bao/3Bao and wild type mice for the embryo of 12.5 days. The W-3Bao/3Bao embryos looked pale since pregnant 14.5 days and dwarf since pregnant 16.5 days. The extremely low level of haematochrome and big red blood cells of W-3Bao/3Bao 18.5-day-embryos were found in the inspections of blood routine items and blood smear, which resulted in death of W-3Bao/3Bao homozygous mouse around being born, and no live postnatal W-3Bao/3Bao mouse was found in this study. No spermatogonium at different developmental stages was found in some contorted seminiferous tubules in adult W-3Bao/+ mouse. At the age of 18.5-day embryo, the spermatogonium of W-3Bao/3Bao mice only lied in interstitial tissue and no one lied in contorted seminiferous tubules, while the spermatogonium of W-3Bao/+ or W+/+ mice lied in interstitial tissue and in contorted seminiferous tubules in the same time. At the age of 18.5-day embryo, cells arranged irregularly and primordial follicles were not seen in the W-3Bao/3Bao ovaries, while primordial follicles appeared clearly in the ovaries of W-3Bao/+ or W+/+ mice. We concluded that because of the nonsense mutation of Kit gene, the W-3Bao/+ mice show white spot and abnormal development of some contorted seminiferous tubules. The W-3Bao/3Bao mice die around birth resulting from severe macrocytic anemia and show abnormal genital glands of both genders.

     

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