scholarly journals Study of polymorphisms in the promoter region of ovine β-lactoglobulin gene and phylogenetic analysis among the Valle del Belice breed and other sheep breeds considered as ancestors

2011 ◽  
Vol 39 (1) ◽  
pp. 745-751 ◽  
Author(s):  
S. Mastrangelo ◽  
M. T. Sardina ◽  
V. Riggio ◽  
B. Portolano
2020 ◽  
Vol 23 (3) ◽  
pp. 295-303
Author(s):  
D. Gencheva

In the present study, single nucleotide polymorphism in exon II of the β-lactoglobulin gene was investigated in four Bulgarian sheep breeds: Bulgarian Dairy Synthetic Population sheep (BDSP), Copper-red Shumen sheep (CRSH), Stara Zagora sheep (STZG) and Pleven Blackhead sheep (PLBH). Two genetic variants of β-LG gene (A and B) have been identified through PCR-RFLP assay. A 103 bp fragment of the polymorphic β-LG locus were amplified and digested with endonuclease enzyme RsaI. The obtained restriction fragments revealed three genotypes: AA, AB and BB, observed in 31%, 65.5% and 3.5% of the BDSP population and in 48%, 28% and 24% of CRSH sheep population, respectively, with departure from the Hardy-Weinberg equilibrium (P<0.05) in these groups. The allele frequencies demonstrated a prevalence of the A allele (0.638 and 0.620) over the B allele (0.362 and 0.380) in both populations. On the contrary, the distribution of allele frequencies in STZG and PLBH was 0.240 and 0.100 for allele A, respectively and 0.760 and 0.900 for allele B. Therefore, the homozygous BB genotype in these sheep populations was more frequently encountered (0.520 and 0.800) than the heterozygous AB genotype (0.480 and 0.200), with HWE correspondence (P>0.1). The homozygous genotype AA was absent in STZG and PLBH sheep populations. The greatest Nei’s genetic distance calculated by UPGMA method was found between the populations BDSPand PLBH (0.5334), while the closest relationship (0.0006) was established between CRSH and BDSP. The results obtained from the present investigation confirmed the presence of the SNP polymorphism in exon II of the β-lactoglobulin gene. Therefore, the genetic variability established in this polymorphic locus could be applied in further association studies with milk production traits in sheep.


2017 ◽  
Vol 17 (2) ◽  
pp. 371-384 ◽  
Author(s):  
Kostas A. Triantaphyllopoulos ◽  
Panagiota Koutsouli ◽  
Athanassios Kandris ◽  
Dimitris Papachristou ◽  
Kalliopi E. Markopoulou ◽  
...  

Abstract The animal selection with favourable phenotypes of the past has been, currently, replaced by the genotype selection on quantitative traits, assisted by the expanding molecular techniques in the context of livestock improvement. In this study, the c.112T>C polymorphism in exon II of β-lactoglobulin (β-LG) gene was investigated in Karagouniko and Chios sheep breeds by using polymerase chain reaction - restriction fragment length polymorphism (PCR-RFLP), and possible associations with milk traits were examined. In total, 125 blood DNA samples were isolated for PCR-RFLP analysis and the respective 217 milk samples′ composition profile was obtained. The goodness of fit test to Hardy-Weinberg equilibrium (HWE) for β-LG genotypes was estimated and associations found between β-LG genotypes and raw milk composition. Two alleles and three genotypes were observed (AA, AB and BB) in both breeds, and Chios breed significantly deviated (P≤0.05) from Hardy-Weinberg equilibrium (HWE). Conclusively, linear mixed model analysis on samples, from both breeds collectively, showed significant effects of β-LG genotype on lactose percentage and somatic cell count (SCC), lactation stage on daily milk yield and protein, while the breed effect was significant only on daily milk yield.


2005 ◽  
Vol 72 (3) ◽  
pp. 379-384 ◽  
Author(s):  
Maria Ballester ◽  
Armand Sánchez ◽  
Josep M Folch

β-lactoglobulin polymorphisms have been reported in the milk of different goat breeds, although no genetic variants affecting the protein have been characterized. In the present study, we amplified and sequenced the proximal promoter and the first six exons containing the entire coding region for the β-lactoglobulin gene in eleven goat breeds from Spain, France, Italy, Switzerland, Senegal and Asia to identify genetic variants. Fifteen polymorphisms were detected, nine in the promoter region and six in the exons of the β-lactoglobulin gene. All polymorphisms were single nucleotide substitutions with the exception of one deletion/insertion in the promoter region. The polymorphisms in the coding region did not produce any amino acid change. In addition, pyrosequencing technology was used to genotype four polymorphisms in the promoter region in 200 goats belonging to eleven breeds. Differences in allelic frequencies for these polymorphisms between breeds are described and a specific polymorphism for the Italian populations was identified. Finally, the analysis of association between these four promoter point mutations was investigated resulting in five haplotypes, GCGC being the most frequent haplotype in all breeds analysed.


Author(s):  
Hong Yao ◽  
Wenbo Zhao ◽  
Dian Jiao ◽  
Stefan Schwarz ◽  
Rongmin Zhang ◽  
...  

Abstract Objectives To investigate the global distribution, dissemination and overexpression of RE-CmeABC in Campylobacter jejuni. Methods WGS information for 433 RE-cmeABC-positive C. jejuni isolates (including 18 isolates sequenced in this study and 415 isolates from GenBank) was used for the generation of minimum-spanning trees with STs. WGS information for 95 representative RE-cmeABC-positive C. jejuni isolates was used for phylogenetic analysis. RT–PCR was conducted to evaluate the association between inverted repeat (IR) sequence diversity in the RE-CmeABC promoter region and RE-cmeABC gene expression. Results WGS analysis revealed the global distribution of RE-cmeABC among C. jejuni from more than 10 countries. MLST results indicated that various STs were involved in the dissemination of RE-cmeABC, with ST2109 being the most predominant ST. Phylogenetic analysis revealed the close relationship between RE-cmeABC-carrying C. jejuni isolates from poultry and humans. The IR polymorphism in the RE-CmeABC promoter region is associated with the overexpression of RE-cmeABC, which was demonstrated experimentally by RT–PCR. Conclusions To the best of our knowledge, our analysis represents the first view of the global distribution of RE-CmeABC, which is horizontally transferable and diffused regionally in a clonal manner. The close relationship of RE-cmeABC-positive C. jejuni from poultry and humans supports the potential of these isolates for zoonotic transmission. Overexpressed RE-CmeABC in C. jejuni will increase the fitness of the corresponding bacteria and be of advantage under antimicrobial selection.


2015 ◽  
Vol 62 (1) ◽  
pp. 109-112 ◽  
Author(s):  
Szilvia Kusza ◽  
Nikolett Sziszkosz ◽  
Krisztina Nagy ◽  
Amela Masala ◽  
Sándor Kukovics ◽  
...  

2010 ◽  
Vol 2 (1) ◽  
pp. 6-9
Author(s):  
G. Elyasi ◽  
J. Shodja ◽  
M.R. Nassiry ◽  
A. Tahmasebi ◽  
O. Pirahary ◽  
...  

2006 ◽  
Vol 44 (7-8) ◽  
pp. 376-381 ◽  
Author(s):  
Cengiz Elmaci ◽  
Yasemin Oner ◽  
M. Soner Balcioglu

2007 ◽  
Vol 32 (2) ◽  
pp. 145-148 ◽  
Author(s):  
Cengiz Elmaci ◽  
Yasemin Oner ◽  
M. S. Balcioglu

2008 ◽  
Vol 8 (4) ◽  
pp. 406-413 ◽  
Author(s):  
Michael E. Steiper ◽  
Sonia J. Parikh ◽  
Julia M. Zichello

2019 ◽  
Vol 99 (2) ◽  
pp. 232-242
Author(s):  
Liping Guo ◽  
Jianzhou Gao ◽  
Jaime A. Teixeira da Silva ◽  
Xiaonan Yu

Auxin plays an important role in various aspects of plant growth and development. Auxin response factors (ARFs) are plant-specific transcription factors that regulate the expression of auxin-responsive genes by binding with auxin response elements (AuxinREs) in the promoter region of such genes. In this study, a genome-wide analysis of the ARF genes in Prunus persica was carried out using the latest updated genomics data of this plant. A total of 17 ARF genes were identified and were named PpARF1 to PpARF17. A comprehensive overview of these PpARFs was undertaken, including a phylogenetic analysis and analysis of gene structures, conserved motifs and domains, chromosome location, cis-elements in the promoter region, and gene expression patterns. The 17 PpARF genes were distributed over eight chromosomes. All identified PpARF proteins had an ARF domain and a typical B3-DNA-binding domain that consisted of two α-helixes and seven β-sheets. Some of the PpARF proteins also had an Aux/IAA domain. Phylogenetic analysis categorized PpARF proteins into four groups. PpARF genes had many elements related to stress responses in the promotor region and showed distinct expression levels in leaves and roots. The present study provides basic information about the ARF gene family in Prunus persica and enables further verification of candidate genes related to plant growth.


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