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XO 小鼠排卵卵母细胞对二倍体的高易感性。

High susceptibility for diploidy in ovulated oocytes from XO mice.

作者信息

Beermann F, Franke U, Hansmann I

出版信息

Hum Genet. 1986 Apr;72(4):323-6. doi: 10.1007/BF00290958.

DOI:10.1007/BF00290958
PMID:3699822
Abstract

Adult female mice of the "sensitive" NMRI/Han strain ovulate diploid oocytes after gonadotropin treatment. Other mouse strains are "non-sensitive" with respect to the ovulation of such diploid oocytes. In this study we combined the impaired ovarian situation in the XO karyotype with the trait "diploidy", which is determined genetically, by mating Ta/O (Ta = Tabby) females of C3H X 101 background to males of the NMRI/Han strain. The adult female F1 hybrids were stimulated to ovulation by gonadotropins and identified by their karyotype (XX or XO). The cytogenetic analysis of ovulated oocytes revealed a low level of diploidy in the XX littermates (1.0%), but a very high level in females with the XO karyotype (24.6%). All of the XO females ovulated at least one diploid oocyte. We suggest that it is the XO status which drastically impairs meiosis I in our "gonadotropin-sensitive" F1 females due to (1) alterations of the developmental program within the oocyte, (2) a disturbed communication between oocyte and follicle, (3) a preferential maturation and ovulation of "follicles at risk", or (4) an exceptional recruitment of many such follicles, by, e.g., a premature responsiveness to gonadotropins in our XO females. An interdependence of several such mechanisms is possible.

摘要

“敏感”的NMRI/Han品系成年雌性小鼠在促性腺激素处理后会排出二倍体卵母细胞。其他小鼠品系对于此类二倍体卵母细胞的排卵则“不敏感”。在本研究中,我们通过将C3H X 101背景的Ta/O(Ta = 虎斑)雌性小鼠与NMRI/Han品系的雄性小鼠交配,把XO核型中受损的卵巢情况与由基因决定的“二倍体”性状结合起来。成年雌性F1杂种小鼠经促性腺激素刺激排卵,并通过其核型(XX或XO)进行鉴定。对排出的卵母细胞进行细胞遗传学分析发现,XX同窝小鼠中二倍体水平较低(1.0%),但XO核型的雌性小鼠中二倍体水平非常高(24.6%)。所有XO雌性小鼠至少排出了一个二倍体卵母细胞。我们认为,正是XO状态在我们“对促性腺激素敏感”的F1雌性小鼠中严重损害了减数分裂I,原因如下:(1)卵母细胞内发育程序的改变;(2)卵母细胞与卵泡之间的通讯紊乱;(3)“处于危险中的卵泡”优先成熟和排卵;或者(4)例如我们的XO雌性小鼠对促性腺激素的过早反应导致许多此类卵泡的异常募集。几种这样的机制之间可能存在相互依存关系。

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2
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引用本文的文献

1
Chromosome segregation at meiosis I in female T(2;4)1Gö/+ mice: no evidence for a decreased crossover frequency with maternal age.雌性T(2;4)1Gö/+小鼠减数分裂I期的染色体分离:没有证据表明随着母龄增加交叉频率降低。
Chromosoma. 1987;95(1):1-7. doi: 10.1007/BF00293834.

本文引用的文献

1
Oocyte depletion in XO mice and their XX sibs from 12 to 200 days post partum.产后12至200天,XO小鼠及其XX同胞的卵母细胞耗竭情况。
J Reprod Fertil. 1981 Jan;61(1):207-12. doi: 10.1530/jrf.0.0610207.
2
Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse.雄激素受体基因座的研究:定位于人类X染色体以及与小鼠Tfm基因座同源性的证据。
Proc Natl Acad Sci U S A. 1981 Oct;78(10):6339-43. doi: 10.1073/pnas.78.10.6339.
3
The use of translocation-derived "marker-bivalents" for studying the origin of meiotic instability in female mice.
利用易位衍生的“标记二价体”研究雌性小鼠减数分裂不稳定性的起源。
Cytogenet Cell Genet. 1980;26(1):49-58. doi: 10.1159/000131421.
4
X-chromosome segregation, maternal age and aneuploidy in the XO mouse.XO小鼠中的X染色体分离、母龄与非整倍体
Genet Res. 1983 Feb;41(1):85-95. doi: 10.1017/s001667230002108x.
5
Absence of correlation between univalent formation and meiotic nondisjunction in aged female Chinese hamsters.老年雌性中国仓鼠单价体形成与减数分裂不分离之间不存在相关性。
Cytogenet Cell Genet. 1983;35(1):34-40. doi: 10.1159/000131833.
6
Ovarian follicle dynamics in mice: a comparative study of three inbred strains and an F1 hybrid.小鼠卵巢卵泡动力学:三种近交系和一个F1杂种的比较研究。
J Endocrinol. 1983 Jan;96(1):23-33. doi: 10.1677/joe.0.0960023.
7
The genetic basis of non-disjunction: increased incidence of hyperploidy in oocytes from F1 hybrid mice.
Hum Genet. 1983;65(1):56-60. doi: 10.1007/BF00285029.
8
Maternal ageing and aneuploid embryos--evidence from the mouse that biological and not chronological age is the important influence.母体衰老与非整倍体胚胎——来自小鼠的证据表明,是生物学年龄而非实际年龄产生重要影响。
Hum Genet. 1984;66(1):41-5. doi: 10.1007/BF00275184.
9
Control of meiosis by somatic cells in mice: inheritance of the meiosis I error 'diploidy' and nonexpression in sensitive NMRI/Han oocytes ovulated from chimeras.小鼠体细胞对减数分裂的控制:减数分裂I错误“二倍体”的遗传以及嵌合体排出的敏感NMRI/Han卵母细胞中该错误的无表达
Cell Differ. 1984 Dec;15(2-4):189-94. doi: 10.1016/0045-6039(84)90074-5.
10
Chemical signals that regulate mammalian oocyte maturation.
Biol Reprod. 1984 Feb;30(1):1-11. doi: 10.1095/biolreprod30.1.1.