Identification of Two Potential Suppressor Gene Regions on Chromosome Arm 14q That Are Commonly Lost in Advanced Colorectal Carcinomas

2001 ◽  
Vol 36 (12) ◽  
pp. 1327-1331 ◽  
Author(s):  
L. Thorstensen, H. Qvist, J. M. Neslan
Author(s):  
Marco Theobald ◽  
Holger Christiansen ◽  
Anke Schmidt ◽  
Badrig Melekian ◽  
Nicole Wolkewitz ◽  
...  

Blood ◽  
1998 ◽  
Vol 92 (6) ◽  
pp. 2113-2117 ◽  
Author(s):  
Yoshihiro Hatta ◽  
Yasuaki Yamada ◽  
Masao Tomonaga ◽  
Jonathan W. Said ◽  
Isao Miyosi ◽  
...  

Allelotype analysis of adult T-cell leukemia (ATL) was undertaken for the first time to identify chromosomal loci relevant to the development of acute/lymphomatous ATL. Loss of heterozygosity (LOH) was screened using 94 highly polymorphic microsatellite markers, distributed among all nonacrocentric, autosomal chromosomes. In each of the 22 cases, DNA obtained from their leukemic cells in acute/lymphomatous phase was compared with their constitutional DNA from mononuclear cells in chronic or remission phase. Allelic losses of at least on one chromosome arm occurred in 91% of the cases (20 individuals). Among 39 chromosome arms, allelic losses were observed on 31 arms at least for one sample. A high frequency of allelic loss (>30%) was seen on chromosome arms 6q (41%) and 17p (48%). The mean fractional allelic loss (FAL) was 0.109. These findings suggest that a novel tumor suppressor gene on chromosome arm 6q, as well as the p53 gene on chromosome arm 17p, probably have an important role in the development of acute/lymphomatous ATL. © 1998 by The American Society of Hematology.


Genome ◽  
1987 ◽  
Vol 29 (4) ◽  
pp. 658-663
Author(s):  
Carla Ceoloni ◽  
Moshe Feldman

Two lines of common wheat cv. Chinese Spring carrying mutant alleles for the Ph2 homoeologous pairing-suppressor gene on chromosome arm 3DS promoting homoeologous pairing in wheat interspecific and intergeneric hybrids have been tested for their mitotic sensitivity to colchicine. Both the ph2a mutation, which corresponds to a fairly long deletion of 3DS, and ph2b, which is either an intragenic change or a very small deletion, as well as the ph2a/ph2b heteroallelic combination and the deficiency for the entire 3DS arm (ditelo 3DL), conditioned a significantly lower sensitivity to colchicine than that determined by the wild-type allele Ph2 (euploid and ditelo 3DS). Observation of both metaphase and anaphse root-tip cell populations, treated with various colchicine concentrations, provided similar results. The degree of spindle disruption in 2 × 10−4 M colchicine, as measured by the percentage of fully affected metaphases (C type), was significantly reduced in ph2 and Ph2− genotypes and, consequently, a larger proportion of cells could proceed toward anaphase and also had a regular segregation pattern at this stage. The differential sensitivity of ph2 genotypes to colchicine is in the opposite direction to that previously found for ph1 genotypes, lacking the homoeologous pairing suppressor on chromosome arm 5BL. The ph2 mutation, while promoting homoeologous pairing as ph1 does, decreases spindle sensitivity to colchicine with respect to the wild-type (ph2) allele rather than increasing it, as ph1 does. The observed alteration of spindle sensitivity to colchicine that mutants for structurally unrelated but functionally related genes (Ph1 and Ph2) condition is interpreted as a highly probable coincidence in their cellular target. It is assumed therefore that these loci affect the equilibrium between tubulin and microtubules. Through this effect they presumably determine chromosome positioning in somatic and premeiotic stages, leading to different pairing patterns at meiosis. Key words: Triticum aestivum, tubulin, pairing suppressors, somatic association.


2000 ◽  
Vol 436 (5) ◽  
pp. 487-493 ◽  
Author(s):  
Julia Reifenberger ◽  
Marietta Wolter ◽  
J. Bostr�m ◽  
Rainer B�schges ◽  
Mosaad Megahed ◽  
...  

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
GiWon Shin ◽  
Stephanie U. Greer ◽  
Erik Hopmans ◽  
Susan M. Grimes ◽  
HoJoon Lee ◽  
...  

AbstractWe developed a sensitive sequencing approach that simultaneously profiles microsatellite instability, chromosomal instability, and subclonal structure in cancer. We assessed diverse repeat motifs across 225 microsatellites on colorectal carcinomas. Our study identified elevated alterations at both selected tetranucleotide and conventional mononucleotide repeats. Many colorectal carcinomas had a mix of genomic instability states that are normally considered exclusive. An MSH3 mutation may have contributed to the mixed states. Increased copy number of chromosome arm 8q was most prevalent among tumors with microsatellite instability, including a case of translocation involving 8q. Subclonal analysis identified co-occurring driver mutations previously known to be exclusive.


Blood ◽  
1998 ◽  
Vol 92 (6) ◽  
pp. 2113-2117 ◽  
Author(s):  
Yoshihiro Hatta ◽  
Yasuaki Yamada ◽  
Masao Tomonaga ◽  
Jonathan W. Said ◽  
Isao Miyosi ◽  
...  

Abstract Allelotype analysis of adult T-cell leukemia (ATL) was undertaken for the first time to identify chromosomal loci relevant to the development of acute/lymphomatous ATL. Loss of heterozygosity (LOH) was screened using 94 highly polymorphic microsatellite markers, distributed among all nonacrocentric, autosomal chromosomes. In each of the 22 cases, DNA obtained from their leukemic cells in acute/lymphomatous phase was compared with their constitutional DNA from mononuclear cells in chronic or remission phase. Allelic losses of at least on one chromosome arm occurred in 91% of the cases (20 individuals). Among 39 chromosome arms, allelic losses were observed on 31 arms at least for one sample. A high frequency of allelic loss (>30%) was seen on chromosome arms 6q (41%) and 17p (48%). The mean fractional allelic loss (FAL) was 0.109. These findings suggest that a novel tumor suppressor gene on chromosome arm 6q, as well as the p53 gene on chromosome arm 17p, probably have an important role in the development of acute/lymphomatous ATL. © 1998 by The American Society of Hematology.


2000 ◽  
Vol 87 (6) ◽  
pp. 798-802 ◽  
Author(s):  
Emma J. Bryan ◽  
Nicola A. Thomas ◽  
Karan Palmer ◽  
Elisabeth Dawson ◽  
Patricia Englefield ◽  
...  

2004 ◽  
Vol 112 (1) ◽  
pp. 150-154 ◽  
Author(s):  
Nozomu Yanaihara ◽  
Michiho Nishioka ◽  
Takashi Kohno ◽  
Ayaka Otsuka ◽  
Aikou Okamoto ◽  
...  

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