268 IDENTIFICATION OF X- AND Y-BEARING SPERMATOZOA IN SORTED BUFFALO (BUBALUS BUBALIS) SEMEN BY FLUORESCENCE IN SITU HYBRIDIZATION

2009 ◽  
Vol 21 (1) ◽  
pp. 231
Author(s):  
M. Zhang ◽  
X. J. Zhuang ◽  
Y. Q. Lu ◽  
C. H. Hu ◽  
S. S. Lu ◽  
...  

Flow cytometry sorting technology has been successfully used to sort the X- and Y-chromosome bearing sperm. Previous studies showed that fluorescence in situ hybridization (FISH) method was a simple and reliable procedure for assessing the effectiveness of separation of X- and Y-sperm in the swine (Kawarasaki T et al. 1998 Theriogenology 50, 625–635) and the bovine (Rens W et al. 2001 Reproduction 121, 541–546). Reports of sex-preselection by flow-cytometry sorting of the X- and Y-sperm were also seen in the buffalo (Presicce GA et al. 2005 Reprod. Dom. Anim. 40, 73–75; Lu YQ et al. 2006 Anim. Reprod. Sci. 100, 192–196). There was, however, no report to date for using the FISH method to assess the purity of the sorted buffalo sperm. The objective of the present study was to verify the purity of flow cytometrically-sorted buffalo X- and Y-sperm by FISH using bovine X- and Y- chromosome painting probes prepared by microdissection. The X- and Y- chromosomes of bovidea were microdissected respectively from the metaphase spreads of Holstein blood cells with a glass needle controlled by a micromanipulator and amplified by degenerate oligo-nucleotide primer-PCR (DOP-PCR) (Mariela N et al. 2005 Genet. Mol. Res. 4, 675–683). The DOP-PCR products of X- and Y- chromosome were labeled with CY3-dUTP and Biotin-11-dUTP, respectively. The buffalo X- or Y-sperm DNA from unsorted semen and sorted semen were hybridized to the labeled probes, respectively. The results showed that the hybridized signals were clearly visible in the metaphase karyotype of bovine and buffalo semen samples. About 47.7% (594/1246) and 48.9% (683/1396) of the unsorted buffalo sperm emitted strong fluorescent signals when assessed by Y- and X-chromosome painting probes, respectively, which was conformed to the sex ratio in normal buffalo sperm (50%:50%). About 86.1% (1529/1776) hybridization signals of the sperm in the sorted X-semen assessed by X-chromosome painting probes were detected, while 82.2% (2232/2716) of the Y-sorted buffalo sperm emitted strong fluorescent signals when assessed by Y-chromosome painting probe. The results of the flow cytometer re-analysis revealed that the proportions of X- and Y-bearing sperm in the sorted semen were 89.6% and 86.7%, respectively. There were no apparent differences between the two assessment methods of sperm separation by flow cytometry re-analysis and by FISH with the X-Y paint probe. In conclusion, bovine X- and Y-chromosome painting probes prepared using microisolation method could be used to verify the purity of the sorted sperm in the buffalo. This study was supported by the Guangxi Department of Science and Technology (0626001-3-1) and National Key Technology R&D Program, The People’s Republic of China (2006BAD04A18). The authors (M. Zhang, X.J. Zhuang, and Y.Q. Lu) contributed equally to this work.

Reproduction ◽  
2001 ◽  
pp. 541-546 ◽  
Author(s):  
W Rens ◽  
F Yang ◽  
G Welch ◽  
S Revell ◽  
PC O'Brien ◽  
...  

X and Y chromosome paints were developed from sorted yak chromosomes for sexing cattle spermatozoa. Clear hybridization signals were obtained for every spermatozoon using a modified sperm decondensation protocol and fluorescence in situ hybridization (FISH). The procedure was evaluated using the established Beltsville sperm sexing technology, which separates spermatozoa by flow cytometry into X- and Y-bearing fractions. Close agreement was found between the assessment of sperm separation by flow cytometry and by FISH with the X-Y paint set. The FISH method is a simple, reliable and robust procedure for assessing the effectiveness of separation of X and Y spermatozoa.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Natalya A. Lemskaya ◽  
Svetlana A. Romanenko ◽  
Yulia V. Maksimova ◽  
Asia R. Shorina ◽  
Dmitry V. Yudkin

Abstract Background The presence of small supernumerary marker chromosomes (sSMCs) in a karyotype leads to diagnostic questions because the resulting extra material may cause abnormal development depending on the origin of the duplication/triplication. Because SMCs are so small, their origin cannot be determined by conventional cytogenetic techniques, and new molecular cytogenetic methods are necessary. Here, we applied a target approach to chromosome rearrangement analysis by isolating a chromosome of interest via microdissection and using it in fluorescence in situ hybridization (FISH) as a probe in combination with whole-chromosome painting probes. This approach allows to identify origins of both the euchromatin and repeat-rich regions of a marker. Case presentation We report a case of an adult male with congenital atresia of the rectum and anus, anotia, and atresia of the external auditory canal along with hearing loss. Karyotyping and FISH analysis with whole-chromosome painting probes of acrocentric chromosomes and the constructed microdissection library of the marker chromosome reliably identified an additional chromosome in some metaphases: mos 47,XY,+idic(22)(q11.2)[14]/46,XY [23]. Conclusion We propose to use whole-chromosome libraries and microdissected chromosomes in FISH to identify SMCs enriched with repeated sequences. We show that the methodology is successful in identifying the composition of a satellited marker chromosome.


Development ◽  
1987 ◽  
Vol 101 (Supplement) ◽  
pp. 41-50
Author(s):  
M. A. Ferguson-Smith ◽  
N. A. Affara ◽  
R. E. Magenis

We have used DNA from 23 patients with Y-chromosome aberrations and 25 patients with presumptive X–Y interchange to map 39 Yp restriction fragments and 37 Yq restriction fragments. In the majority of patients the results are consistent with a standard contiguous order of sequences along the Y chromosome. In 6 of 26 patients (23 %) with Yp aberrations and 2 of 17 (12 %) with Yq aberrations, exceptions to the consensus order have been observed. These can be accommodated by postulating the presence of inversion polymorphisms. Such variation may occur more commonly on the nonpairing part of the Y chromosome that in other chromosomes owing to the absence of homologous synapsis and recombination in male meiosis. The Y sequence most frequently present in X–Y interchange males was that recognized by GMGY3. 18 of 19 X–Y interchange males had this sequence suggesting that it is the nearest in the series to the TDF locus, and indicating that the latter maps to the distal end of Yp. Several techniques, including in situ hybridization and DNA measurement by flow cytometry, have been used to demonstrate that in X–Y interchange males there is transfer of Y sequences to the distal end of the X chromosome; no mechanism other than X–Y interchange has been demonstrated.


1993 ◽  
Vol 47 (8) ◽  
pp. 1153-1156 ◽  
Author(s):  
Alessandra M. V. Duncan ◽  
Athen Macdonald ◽  
Carolyn J. Brown ◽  
Daynna Wolff ◽  
Huntington F. Willard ◽  
...  

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