PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 15, 2003Molecular Reproduction and Development13 citations

Frequency of recombinant and nonrecombinant products of pericentric inversion of chromosome 1 in sperm nuclei of carrier: By FISH technique

View Full Paper
TYTahsin YakutHAHasan AcarÜEÜnal Egelí

Key Points

Key points are not available for this paper at this time.

Abstract

Meiotic segregation products of carriers with pericentric inversion are very important for assessing the risk of unbalanced forms and appropriate genetic counseling. We investigated the incidence of recombinant and nonrecombinant products of chromosome 1 with pericentric inversion, in the sperm nuclei of the carrier by using triple color fluorescence in situ hybridization (FISH). The centromere specific and telomere specific probes for chromosome 1 were used. In the segregation analysis, 1,636 sperm nuclei were analyzed; 82.5% of the sperms were including normal or inverted chromosome 1, and the dup(p)/del(q) and del(p)/dup(q) recombinant products in sperm nuclei of our carrier were 8.7 and 7.3%, respectively. The number of recombinant products may be dependent on the formation of an inversion loop, which the number of the formation of chiasmata results in the different number of normal/balanced and recombinant products. The use of FISH, using different probe combination, in sperm nuclei has proved to be an accurate approach to determine the meiotic segregation patterns and could help to better establish a reproductive prognosis and genetic counseling.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Yakut et al. (2003) studied this question.

synapsesocial.com/papers/6a00e4da4716aad0cc85dcbdhttps://doi.org/10.1002/mrd.10325
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Analysis of chiasma frequency and first meiotic segregation in a human male reciprocal translocation heterozygote, t(1;11) (p36.3;q13.1), using fluorescence in situ hybridisation2008 · 56 citations
  2. 2Prenatal diagnosis of a fetus with pure partial trisomy 1q32‐44 due to a familial balanced rearrangement2002 · 20 citations
  3. 3Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion, inv(8)(p23q22)2008 · 27 citations
  4. 4The Impact of Aneuploidy Upon Public Health: Mortality and Morbidity Associated with Human Chromosome Abnormalities1985 · 90 citations
  5. 5G-band position effects on meiotic synapsis and crossing over.1988 · 89 citations