14 Telomere length in cloned camels produced by somatic cell nuclear transfer is not different from that in their naturally produced counterparts

2021 ◽  
Vol 33 (2) ◽  
pp. 114
Author(s):  
N. A. Wani ◽  
K. P. Kumar

There are controversial reports on the restoration of eroded telomere length in offspring produced by somatic cell nuclear transfer (SCNT) in different animal species. To the best of our knowledge, no earlier studies report telomere length in naturally produced or cloned animals in any of the camelid species. Therefore, the present study was conducted to estimate the telomere length in dromedary camels produced by SCNT, and their age-matched naturally produced counterparts by terminal restriction fragment (TRF) analysis. Genomic DNA was extracted from venous blood collected from 6 cloned animals (aged 3, 12, and 24 months), and their age-matched counterparts by a conventional phenol/chloroform protocol. Denatured and neutralized DNA was blotted onto a positively charged nylon membrane and fixed by baking at 80°C for 3h. After washing in a prewarmed digoxigenin (DIG) easy hybridization solution at 42°C for 1h, DNA hybridization was carried out using a telomere (TTAGGG)n-specific, DIG-labelled hybridization probe (Roche Diagnostics, Germany) at 42°C for 4h. Stringent washes were carried out at the same temperature, followed by chemiluminescence reaction. The signals were captured using the Azure Biosystems C600 gel documentation system. Molecular weights of the unknown TRF bands on the gel were calculated using known molecular weight marker provided by Telo TAGGG Telomere Length Assay Kit (Roche Diagnostics). A TeloTool program from MATLAB software with a built-in probe intensity correction algorithm was used for TRF analysis. The experiment was replicated 3 times, and the data, presented as mean±s.e.m., were analysed using a 2-sample t-test (Minitab statistical software). No difference (P>0.05) was found in the mean telomere length of cloned camels compared with their naturally produced age-matched counterparts (21.7±0.3 vs. 22.1±0.3; 21.9±0.3 vs. 22.1±0.3; 22.2±0.5 vs. 22.0±0.1; 20.5±0.5 vs. 22.5±0.7; 20.1±0.1 vs. 22.5±0.7; 21.7±1.1 vs. 22.6±0.2), respectively. In conclusion, this is the first study where telomere length has been reported in naturally produced and cloned dromedary camels produced by SCNT. We found that telomere lengths in cloned camels were similar to those of their age-matched naturally produced counterparts, suggesting that the camel cytoplast reprograms the somatic cell nucleus and restores the telomere length to its totipotency stage.

2008 ◽  
Vol 54 (4) ◽  
pp. 254-258 ◽  
Author(s):  
Mayuko KUROME ◽  
Hisashi HISATOMI ◽  
Shirou MATSUMOTO ◽  
Ryo TOMII ◽  
Satoshi UENO ◽  
...  

2004 ◽  
Vol 16 (2) ◽  
pp. 134
Author(s):  
B. Alexander ◽  
S. Perrault ◽  
T. Peura ◽  
D.H. Betts ◽  
W. A. King

The technique of somatic cell nuclear transfer (SCNT) involves the transplantation of a cultured somatic cell into an enucleated oocyte. Following activation, the nucleus of the somatic cell should be reprogrammed to a state of totipotency, which involves the resetting of epigenetic modifications of the somatic genome and also rebuilding of the chromosomal ends (telomeres). This study was carried out to investigate whether the nuclear transfer technique could rebuild the telomeres in sheep clones and their offspring when compared to age-matched control animals. Skin and blood samples were collected from three SCNT-derived sheep clones, and three of their offspring generated by natural mating. Control samples were collected from age-matched animals (n=17), spanning an age range from 1 month to 36 months of age. Ovine genomic DNA was extracted from samples using a Qiagen DNA extraction kit according to the manufacturer’s instructions. TeloTAGGG telomere length chemiluminescent assay kit (Roche Diagnostics) was used to determine the telomere length of all samples. Samples of ovine genomic DNA (2mg) were digested at 37°C for 2h using Hinf 1 and Rsa 1 endonuclease master-mix at the rate of 40 IU per sample. The resulted terminal restriction fragments (TRF) were separated on 1.2% agarose gel by pulsed field electrophoresis at 6V with 0.1s switch time for 4h in 0.5% TBE buffer at 14°C. The DNA fragments were southern-transferred to a nylon membrane and hybridized with telomere-specific (TTAGGG)n, digoxigenin (DIG)-labeled hybridization probe at 42°C. Following post-hybridization washes the membrane was incubated with DIG-specific antibody covalently coupled to alkaline phosphatase. The immobilized telomere probe was visualized by adding a chemiluminecence substrate to the membrane and exposed to X-ray film. Mean TRF length was determined by comparing the telomere densitometry signals to a molecular weight standard. High resolution bands resulting from pulsed field gel electrophoresis revealed that ovine TRF size distribution was in the range of 10–19kb. Linear regression analysis resulted in significant (t=25.84, P<0.05) decrease of mean TRF size with increasing age, at a mean rate of 0.08kb per every 6 months. Mean TRF length of SCNT-derived sheep clones, Matilda (28 months old), Macather (14 months old) and Frida (13 months old) were 11.12kb, 11.40kb, and 13.41kb, respectively. Their mean TRF values were significantly (P<0.05) shorter than those of their age-matched control animals: 16.95kb, 14.76kb, and 14.76kb, respectively (n=3 per group). The mean TRF length of the 3 offspring (21 months old) derived from natural mating was not significantly (P<0.05) different from age-matched controls (17.75±0.69kb v. 16.28±0.72kb). These results demonstrate that sheep clones derived from cultured somatic cells have shorter telomere lengths compared to age-matched controls, but this telomere loss is reset in the subsequent generation through natural breeding of the clones. (Funded by NSERC, OMAFRA and International Council for Canadian Studies.)


2009 ◽  
Vol 21 (1) ◽  
pp. 117
Author(s):  
S. G. Hong ◽  
J. E. Park ◽  
J. T. Kang ◽  
H. J. Oh ◽  
M. J. Kim ◽  
...  

Several cloned dogs have been successfully produced by somatic cell nuclear transfer. However, there is no investigation of its reproductive characteristics including changes of hormone and ovarian follicles in cloned dogs. Thus, this study was to examine the onset of puberty, follicular dynamics, and reproductive hormone profiles in cloned beagle dogs. Two female cloned beagles, derived from fetal fibroblasts, were compared to 2 individual age- and weight-matched female beagles produced by natural breeding. All dogs were examined twice weekly from 6 months for the presence of swelling of the vulva and serosanguineous vaginal discharge, which were used as markers of the onset of proestrus. From the first day of proestrus, jugular venous blood samples were collected twice a day for hormonal analysis. Also, from the day when progesterone concentration was >1 ng mL–1 until 5 days after ovulation, blood sampling was carried out 3 times a day. Ultrasound examination of ovaries and uterus was performed daily from the onset of proestrous until 5th day post-ovulation. Cloned female dogs (332.5 ± 1.5 days) reached puberty later than controls (300 ± 8 days). The mean number of ovarian follicles was 4.5 ± 0.5 v. 6.5 ± 0.5 for clones and controls, respectively. The largest size of ovarian follicles in clones and controls detected by ultrasound were 0.6 ± 0.03 v. 0.69 ± 0.07 cm, respectively. It took 8 days from the initiation of vulvar bleeding to the LH peak in all beagles. Moreover, there were no differences in the profile of hormonal changes (LH, FSH, estradiol, and progesterone) in cloned and control beagles. These results demonstrate that cloned dogs have normal development of reproduction. This study was financially supported by the Korean MEST, through KOSEF (grant # M10625030005-08N250300510) and the BK21 program for Veterinary Science.


2012 ◽  
Vol 14 (1) ◽  
pp. 79-87 ◽  
Author(s):  
Sumeth Imsoonthornruksa ◽  
Anawat Sangmalee ◽  
Kanokwan Srirattana ◽  
Rangsun Parnpai ◽  
Mariena Ketudat-Cairns

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