Regulatory single nucleotide polymorphisms at the beginning of intron 2 of the human KRAS gene

Bibliographische Detailangaben
Parent link:Journal of Biosciences
Vol. 407, iss. 5.— 2015.— [P. 873-883]
Körperschaft: Национальный исследовательский Томский политехнический университет Физико-технический институт Кафедра прикладной физики (№ 12)
Weitere Verfasser: Antontseva E. V. Elena Vyacheslavovna, Matveeva M. Yu. Marina Yurjevna, Bondar N. P. Natalia Petrovna, Kashina E. V. Elena Valentinovna, Leberfarb E. Yu. Elena Yurjevna, Bryzgalov L. O. Leonid Olegovich, Gervas P. A. Polina Anatolevna, Ponomareva A. A. Anastasiya Alekseevna, Cherdyntseva N. V. Nadezhda Viktorovna, Orlov Yu. L. Yury Lvovich, Merkulova T. I. Tatjyana Ivanovna
Zusammenfassung:Title screen
There are two regulatory single nucleotide polymorphisms (rSNPs) at the beginning of the second intron of the mouse K-ras gene that are strongly associated with lung cancer susceptibility. We performed functional analysis of three SNPs (rs12228277: T>A, rs12226937: G>A, and rs61761074: T>G) located in the same region of human KRAS. We found that rs12228277 and rs61761074 result in differential binding patterns of lung nuclear proteins to oligonucleotide probes corresponding two alternative alleles; in both cases, the transcription factor NF-Y is involved. G>A substitution (rs12226937) had no effect on the binding of lung nuclear proteins. However, all the nucleotide substitutions under study showed functional effects in a luciferase reporter assay. Among them, rs61761074 demonstrated a significant correlation with allele frequency in non-small-cell lung cancer (NSCLC). Taken together, the results of our study suggest that a T>G substitution at nucleotide position 615 in the second intron of the KRAS gene (rs61761074) may represent a promising genetic marker of NSCLC.
Режим доступа: по договору с организацией-держателем ресурса
Sprache:Englisch
Veröffentlicht: 2015
Schlagworte:
Online-Zugang:http://dx.doi.org/10.1007/s12038-015-9567-8
Format: Elektronisch Buchkapitel
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=649028

MARC

LEADER 00000naa0a2200000 4500
001 649028
005 20250227144355.0
035 |a (RuTPU)RU\TPU\network\14189 
090 |a 649028 
100 |a 20160616d2015 k||y0rusy50 ba 
101 0 |a eng 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Regulatory single nucleotide polymorphisms at the beginning of intron 2 of the human KRAS gene  |f E. V. Antontseva [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 50 tit.] 
330 |a There are two regulatory single nucleotide polymorphisms (rSNPs) at the beginning of the second intron of the mouse K-ras gene that are strongly associated with lung cancer susceptibility. We performed functional analysis of three SNPs (rs12228277: T>A, rs12226937: G>A, and rs61761074: T>G) located in the same region of human KRAS. We found that rs12228277 and rs61761074 result in differential binding patterns of lung nuclear proteins to oligonucleotide probes corresponding two alternative alleles; in both cases, the transcription factor NF-Y is involved. G>A substitution (rs12226937) had no effect on the binding of lung nuclear proteins. However, all the nucleotide substitutions under study showed functional effects in a luciferase reporter assay. Among them, rs61761074 demonstrated a significant correlation with allele frequency in non-small-cell lung cancer (NSCLC). Taken together, the results of our study suggest that a T>G substitution at nucleotide position 615 in the second intron of the KRAS gene (rs61761074) may represent a promising genetic marker of NSCLC. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Journal of Biosciences 
463 |t Vol. 407, iss. 5  |v [P. 873-883]  |d 2015 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
701 1 |a Antontseva  |b E. V.  |g Elena Vyacheslavovna 
701 1 |a Matveeva  |b M. Yu.  |g Marina Yurjevna 
701 1 |a Bondar  |b N. P.  |g Natalia Petrovna 
701 1 |a Kashina  |b E. V.  |g Elena Valentinovna 
701 1 |a Leberfarb  |b E. Yu.  |g Elena Yurjevna 
701 1 |a Bryzgalov  |b L. O.  |g Leonid Olegovich 
701 1 |a Gervas  |b P. A.  |g Polina Anatolevna 
701 1 |a Ponomareva  |b A. A.  |c biologist  |c expert of Tomsk Polytechnic University, candidate of biological sciences  |f 1985-  |g Anastasiya Alekseevna  |3 (RuTPU)RU\TPU\pers\36792  |9 19821 
701 1 |a Cherdyntseva  |b N. V.  |g Nadezhda Viktorovna 
701 1 |a Orlov  |b Yu. L.  |g Yury Lvovich 
701 1 |a Merkulova  |b T. I.  |g Tatjyana Ivanovna 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Физико-технический институт  |b Кафедра прикладной физики (№ 12)  |3 (RuTPU)RU\TPU\col\18729  |9 27178 
801 2 |a RU  |b 63413507  |c 20160616  |g RCR 
856 4 0 |u http://dx.doi.org/10.1007/s12038-015-9567-8 
942 |c CF