Flow cytometric method for measuring chromatin fragmentation in fixed sperm from yellow perch (Perca flavescens)

J. A. Jenkins, R. O. Draugelis-Dale, A. E. Pinkney, L. R. Iwanowicz, Vicki Suzette Blazer

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Declining harvests of yellow perch, Perca flavescens, in urbanized watersheds of Chesapeake Bay have prompted investigations of their reproductive fitness. The purpose of this study was to establish a flow cytometric technique for DNA analysis of fixed samples sent from the field to provide reliable gamete quality measurements. Similar to the sperm chromatin structure assay, measures were made on the susceptibility of nuclear DNA to acid-induced denaturation, but used fixed rather than live or thawed cells. Nuclei were best exposed to the acid treatment for 1minute at 37°C followed by the addition of cold (4°C) propidium iodide staining solution before flow cytometry. The rationale for protocol development is presented graphically through cytograms. Field results collected in 2008 and 2009 revealed DNA fragmentation up to 14.5%. In 2008, DNA fragmentation from the more urbanized watersheds was significantly greater than from reference sites (P=0.026) and in 2009, higher percentages of haploid testicular cells were noted from the less urbanized watersheds (P=0.032) indicating better reproductive condition at sites with less urbanization. For both years, total and progressive live sperm motilities by computer-assisted sperm motion analysis ranged from 19.1% to 76.5%, being significantly higher at the less urbanized sites (P<0.05). This flow cytometric method takes advantage of the propensity of fragmented DNA to be denatured under standard conditions, or 1minute at 37°C with 10% buffered formalin-fixed cells. The study of fixed sperm makes possible the restrospective investigation of germplasm fragmentation, spermatogenic ploidy patterns, and chromatin compaction levels from samples translocated over distance and time. The protocol provides an approach that can be modified for other species across taxa.

Original languageEnglish (US)
Pages (from-to)920-931
Number of pages12
JournalTheriogenology
Volume83
Issue number5
DOIs
StatePublished - Mar 15 2015

Fingerprint

Perches
Perca flavescens
Chromatin
chromatin
Spermatozoa
DNA fragmentation
spermatozoa
DNA Fragmentation
DNA
Genetic Fitness
Urbanization
Acids
Propidium
Sperm Motility
Ploidies
Haploidy
Chesapeake Bay
cells
sperm motility
acid treatment

All Science Journal Classification (ASJC) codes

  • Small Animals
  • Food Animals
  • Animal Science and Zoology
  • Equine

Cite this

Jenkins, J. A. ; Draugelis-Dale, R. O. ; Pinkney, A. E. ; Iwanowicz, L. R. ; Blazer, Vicki Suzette. / Flow cytometric method for measuring chromatin fragmentation in fixed sperm from yellow perch (Perca flavescens). In: Theriogenology. 2015 ; Vol. 83, No. 5. pp. 920-931.
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abstract = "Declining harvests of yellow perch, Perca flavescens, in urbanized watersheds of Chesapeake Bay have prompted investigations of their reproductive fitness. The purpose of this study was to establish a flow cytometric technique for DNA analysis of fixed samples sent from the field to provide reliable gamete quality measurements. Similar to the sperm chromatin structure assay, measures were made on the susceptibility of nuclear DNA to acid-induced denaturation, but used fixed rather than live or thawed cells. Nuclei were best exposed to the acid treatment for 1minute at 37°C followed by the addition of cold (4°C) propidium iodide staining solution before flow cytometry. The rationale for protocol development is presented graphically through cytograms. Field results collected in 2008 and 2009 revealed DNA fragmentation up to 14.5{\%}. In 2008, DNA fragmentation from the more urbanized watersheds was significantly greater than from reference sites (P=0.026) and in 2009, higher percentages of haploid testicular cells were noted from the less urbanized watersheds (P=0.032) indicating better reproductive condition at sites with less urbanization. For both years, total and progressive live sperm motilities by computer-assisted sperm motion analysis ranged from 19.1{\%} to 76.5{\%}, being significantly higher at the less urbanized sites (P<0.05). This flow cytometric method takes advantage of the propensity of fragmented DNA to be denatured under standard conditions, or 1minute at 37°C with 10{\%} buffered formalin-fixed cells. The study of fixed sperm makes possible the restrospective investigation of germplasm fragmentation, spermatogenic ploidy patterns, and chromatin compaction levels from samples translocated over distance and time. The protocol provides an approach that can be modified for other species across taxa.",
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Flow cytometric method for measuring chromatin fragmentation in fixed sperm from yellow perch (Perca flavescens). / Jenkins, J. A.; Draugelis-Dale, R. O.; Pinkney, A. E.; Iwanowicz, L. R.; Blazer, Vicki Suzette.

In: Theriogenology, Vol. 83, No. 5, 15.03.2015, p. 920-931.

Research output: Contribution to journalArticle

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