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PMID: 6746622 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Isolation and characterization of TH3, a germ cell-specific variant of histone 3 in rat testis.

The Journal of biological chemistry ·Vol. 259 ·No. 14 ·1984-07-25 ·Pages 8769-76

Trostle-Weige PK, Meistrich ML, Brock WA, Nishioka K

Abstract

We have identified and purified TH3, a germ cell-specific histone. It has been characterized by amino acid analysis, tryptic peptide mapping, labeling with cystine, and by electrophoretic mobility as a variant of H3. On fully reduced Triton/acid/urea gels its mobility is retarded more than that of the somatic variants H3.2 and H3.3, but less than that of H3.1; it migrates between the H2As and H1s. Germinal cells from adult and sexually immature testes were purified by centrifugal elutriation followed by Percoll density gradient separation in order to study the distribution and synthesis of TH3. TH3 is found in significant levels in spermatogonia and in similar or slightly higher amounts in spermatocytes and round spermatids. The synthesis of TH3 takes place in the spermatogonia but not in spermatocytes, in contrast to the other testis-specific histones, TH2A, H1t, and TH2B. Therefore, TH3 may have a different role in spermatogenesis than do the other testis-specific histone variants.

MeSH Terms
Amino Acids/analysis Animals Electrophoresis, Polyacrylamide Gel Genetic Variation Histones/genetics,isolation & purification Male Molecular Weight Peptide Fragments/analysis Rats Rats, Inbred Strains Testis/metabolism Trypsin
Chemicals
Amino Acids Histones Peptide Fragments Trypsin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Trostle-Weige P K
Meistrich M L
Brock W A
Nishioka K
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1984-07-25
Pages
8769-76
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NICHD NIH HHS · HD-16843 · United States
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