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A N Tomilin

Publications and source records attributed to A N Tomilin.

5 recordsLinked to original sources

[Organization of DNA replication domains in S-phase nuclei of human cells].

Each chromosome of eukaryotic cells contains multiple units of DNA replication that are activated during S-phase of cell cycle according to a definite program. It is considered at present that the main independent units of replication in mammalian cells represent groups of 20-25 adjacent synchronously activated small (with the average size 100 kbp) replicons. After labelling of nascent DNA with nonradioactive DNA precursors and immunofluorescent staining of incorporated label, discrete replication domains (RDs) are detected in S-phase nuclei. It is assumed that each RD is formed by a single group of synchronously activated small replicons. Since the average rate of replication fork movement is 2 kbp/min, a group of small replicons should finish DNA synthesis within 25 min, and only during this time one RD should incorporate the replicative label. We have studied the duration of DNA synthesis in individual RDs in S-phase human cells using double replicative labelling that can be detected in the nucleus by specific reagents. Our results indicate that in the main fraction of RDs DNA synthesis lasts more than 90 min, that contradicts the generally accepted model of organization of replication units in mammalian cells (Hand, 1978), but is in agreement with an alternative model, according to which the main replication units are single or clustered big replicons more than 300 kbp in size (Liapunova, 1994).

Cell Nucleus↗

[An immunohistochemical study of the expression of transcription factor Oct3/4 in mouse spermatogenesis].

The expression of POU-domain transcription factor Oct3/4 in the testis of adult mice has been studied using indirect immunofluorescence with highly specific antibodies. The protein is shown to be expressed in germ cells of seminiferous epithelium in a stage specific manner. The protein synthesis is initiated in mid-pachytene spermatocytes, increases to reach its peak during meiotic division. The Oct3/4 level remains augmented in early spermatids, but gradually declines during their further developmental advancement. These findings imply that Oct3/4 may have a regulatory function providing for the control of meiosis and/or terminal differentiation of spermatogenic cells.

Animals↗

Human male infertility may be due to a decrease of the protamine P2 content in sperm chromatin.

Basic chromosomal proteins were extracted from the sperm of fertile and infertile human males. The relative proportions of protamine 1, 2, and 3 were determined by scanning microdensitometry following electrophoresis of total protamine in polyacrylamide gels. The findings were as follows: (1) The proportion of protamine P(2 + 3) in sperm obtained from infertile males was lower than that in fertile males. (2) Protamine P(2 + 3) in infertile human males showed reduced affinity to DNA. The possibility that some cases of human male infertility may be due to mutation within the protamine P2 gene is discussed.

Chromatin↗

[Human male sterility can be caused by mutations in the protamine P2 gene].

The sperm of fertile and infertile human males was treated with 0.25 n. HCl or 1% CTAB. Relative proportions of various protamine fractions in the obtained extracts were determined by scanning microdensitometry following electrophoresis of the total protamine in polyacrilamide gels. The findings were as follow. 1. The share of protamine P(2 + 3) in the sperm obtained from infertile males was lower than that of fertile males. 2. Protamine P2 in infertile males has a reduced affinity to DNA. It is suggested that in some cases the human male infertility may be due to some mutations within the P2 gene.

Cell Count↗