Summary
The addition of thymidine (TdR) to cells growing in a medium containing 5-bromodeoxyuridine (BUdR) at the end of the first replication cycle results in the incorporation of TdR into the late replicating DNA regions.
These sites can be visualized by staining the metaphase chromosomes with the fluorescent dye “33 258 Hoechst” or a “33 258 Hoechst” Giemsa procedure.
A sequence of late replication patterns has been established in metaphase chromosomes of cultured human peripheral lymphocytes.
The patterns are in agreement with those obtained by the standard autoradiographic procedures, but are more accurate. As is known from autoradiography, late replicating bands are in the position of G or Q bands.
The “33 258 Hoechst” Giemsa staining procedure of chromosomes which have replicated in the presence of BUdR first and in TdR for the last 2 hrs of the S phase is preferable to the currently used Giemsa banding techniques: the method yields very well banded metaphases in all preparations examined, as the chromosome structure is not disrupted by the pretreatment. The bands are very distinct, even in the “difficult” chromosomes (e.g No. 4, 5, 8, and X). In female cells the late replicating X chromosome can be identified by its size and staining pattern.
In addition to the replication asynchrony, the sequence of replication within both X chromosomes in female cells is not absolutely identical.
The phenomenon of a phase difference in replication between the homologues is not a peculiarity of the X chromosome, but can be found in all autosomes as well as in homologous positions on the chromatids of individual chromosomes.
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Grzeschik, K.H., Kim, M.A. & Johannsmann, R. Late replicating bands of human chromosomes demonstrated by fluorochrome and Giemsa staining. Hum Genet 29, 41–59 (1975). https://doi.org/10.1007/BF00273350
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DOI: https://doi.org/10.1007/BF00273350