Timing of the first cleavage division of the mouse and the duration of its component stages: a study of living and fixed eggs.

نویسنده

  • M H Kaufman
چکیده

Fertilized mouse eggs were examined between 27 and 34 h after the superovulating injection of human chorionic gonadotrophin (HCG). Out of 1334 eggs examined, 432 were already at the 2-cell stage; the remaining 902 at the i-cell stage were examined in detail. All chromosome preparations of the first cleavage mitosis were classified into groups corresponding with the stages of prometaphase (early and late), metaphase (early or 'prechromatid', 'chromatid' and 'late chromatid') and anaphase. An indirect estimate was made of the duration of the first cleavage mitosis and of its component stages from the incidence of stages observed at different time intervals after the HCG injection. Fertilized eggs were also observed at 37 C by time-lapse cine-photography and the interval between the disappearance of the pronuclei and the beginning of telophase of the first cleavage division was determined. The progress of eggs fertilized in vitro was also observed under normal culture conditions. A close correlation was observed between the indirect method of assessing die mitotic time and the direct values obtained from the studies on time-lapse and in vitro culture. The effect of temperature on the mitotic time was also examined by the timelapse method.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Timing of the first cleavage division of haploid mouse eggs, and the duration of its component stages.

Mouse eggs were activated by treatment with hyaluronidase which removed the follicle cell9, followed by culture in vitro, and examined at the first cleavage mitosis. Second polar body extrusion usually occurred and haploid parthenogenesis was initiated. Air-dried chromosome preparations were made between 11 and 15-5 h after activation. Out of the 308 eggs examined 74 had already progressed to t...

متن کامل

Timing of The First Zygotic Cleavage Affects Post-Vitrification Viability of Murine Embryos Produced In Vivo

Background Timing of the first zygotic cleavage is an accurate predictor of embryo quality. Embryos that cleaved early (EC) have been shown to exhibit higher developmental viability compared to those that cleaved at a later period (LC). However, the viability of EC embryos in comparison to LC embryos after vitrification is unknown. The present study aims to investigate the post-vitrification de...

متن کامل

The effects of dimethyl sulfoxide and ethylene glycol as vitrification protectants on different cleavage stages of mouse embryo quality

The effect of modified vitrification was assessed on cellular development capability in mouse embryos cultured in vitro. In this study, 466 embryos (from zygote to morula stages) were vitrified then thawed embryos have been incubated for in vitro farther development up to blastocyst stage. Also, vitrification and thawing procedures were the same for all experimental groups. Mouse different embr...

متن کامل

Internal Traits of Eggs and Their Relationship to Shank Feathering in Chicken Using Principal Component Analysis

Chicken eggs represent an important source of protein to the growing human population and also supply repositories of unique genes that could be used worldwide. The inheritance of shank feathering trait is dominant upon non-feathering shank trait in chicken which is based on two factors: pti-1L and pti-1B that are located on Chromosomes 13, 15, and 24. Using 185 fertile eggs collected from two ...

متن کامل

Detection of Glycoconjugate Changes in the Embryonic Trigeminal Nucleus in Balb/C Mouse by Lectin Histochemistry

Purpose: Determination of changes of glycoconjugates, which have special terminal sugars, in embryonic developmental processes of brain stem and trigeminal nucleus in Balb/C mouse. Materials and Methods: In this study mice embryos between 10-17 embryonic days were used. They were fixed according to ordinary laboratory procedures. The specimens were embedded in paraffin and serial sections with...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Journal of cell science

دوره 12 3  شماره 

صفحات  -

تاریخ انتشار 1973