2006
DOI: 10.1159/000095237
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Chromosome ideograms of the laboratory rat <i>(Rattus norvegicus)</i> based on high-resolution banding, and anchoring of the cytogenetic map to the DNA sequence by FISH in sample chromosomes

Abstract: A detailed banded ideogram representation of the rat chromosomes was constructed based on actual G-banded prometaphase chromosomes. The approach yielded 535 individual bands, a significant increase compared to previously presented ideograms. The new ideogram was adapted to the existing band nomenclature. The gene locus positions in the rat draft DNA sequence were compared to the chromosomal positions as determined by dual-color FISH, using rat (RNO) chromosomes 6 and 15 and a segment of RNO4 as sample regions.… Show more

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Cited by 21 publications
(17 citation statements)
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“…RNO6 painting and the rat PAC clone RP31- 202O5 were used to access the amplification status of Mycn . RP31-202O5 was earlier confirmed to contain Mycn gene and mapped to RNO 6q15.3-16 [23] and was also used in this work for the accurate identification of HH-16 cl.2/1 breakpoint regions. During HH-16 cl.2/1 cytogenetic characterization, it was possible to verify that this gene was present in three copies distributed among two intact RNO6 chromosomes and in the derivative chromosomes der(19)t(6;19)(q14;q12), der(18;19)t(18;19)(p10,q10)t(6;19)(q14;q12),der(19)t(6;19)(q14;q12) and der(19)t(4;19)(q31;p11)t(6;19)(q14;q12), indicating that a partial trisomy of RNO6 was involved in a translocation.…”
Section: Resultsmentioning
confidence: 90%
See 1 more Smart Citation
“…RNO6 painting and the rat PAC clone RP31- 202O5 were used to access the amplification status of Mycn . RP31-202O5 was earlier confirmed to contain Mycn gene and mapped to RNO 6q15.3-16 [23] and was also used in this work for the accurate identification of HH-16 cl.2/1 breakpoint regions. During HH-16 cl.2/1 cytogenetic characterization, it was possible to verify that this gene was present in three copies distributed among two intact RNO6 chromosomes and in the derivative chromosomes der(19)t(6;19)(q14;q12), der(18;19)t(18;19)(p10,q10)t(6;19)(q14;q12),der(19)t(6;19)(q14;q12) and der(19)t(4;19)(q31;p11)t(6;19)(q14;q12), indicating that a partial trisomy of RNO6 was involved in a translocation.…”
Section: Resultsmentioning
confidence: 90%
“…The selected clones contained regions of rat chromosomes 6 (RP31-262B4, CH230-208E5, RP31- 202O5, RP31-039D3, CH230-10B5) and 15 (CH230-174M18, CH230-9A5, CH230-215E5, CH230-27O13, CH230-165C24, CH230-117H20), which were physically mapped in a previous study [23]. The BAC/PAC results allowed the identification of the breakpoint regions of the derivative chromosomes involving RNO6 to der(19)t(6;19)(q14;q12), der(19)t(4;19)(q31;p11)t(6;19)(q14;q12) and der(18;19)t(18;19)(p10,q10)t(6;19)(q14;q12), assigning the location of the breakpoint in all of these chromosomes to band 6q14, above the region included within clone RP31-262B4 (Figure 3).…”
Section: Resultsmentioning
confidence: 99%
“…The majority of tumors displayed a complex pattern of numerical and structural aberrations (Figure 1). Using the International System for Human Cytogenetic Nomenclature (ISCN 1995) and literature on nomenclature for G-bands in rat chromosome [25,26], we determined the most common cytogenetic changers among the tumors (Table 2). …”
Section: Resultsmentioning
confidence: 99%
“…The study of an organism genome at the chromosomal level can be used in differentiating one species from another, i.e., the analysis of chromosome numbers, size, and centromere positions [11,12,13]. In fact, modern cytogenetic techniques have since mid-1990s been adopted for studies of Gastropoda.…”
mentioning
confidence: 99%