• 식물분류학회지
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• 제39권1호
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• pp.42-47
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• 2009

본 연구에서 한국산 갈퀴덩굴속(Galium) 14 분류군의 체세포염색체수를 밝혔다. 본 속의 체세포염색체수는 2n = 22, 24, 44, 48, 66, 72, 77, 88로 나타났으며, 기본염색체수는 x = 11, 12로 확인되었다. x = 11의 기본염색체수를 갖는 분류군들은 2배체, 4배체, 7배체, 8배체의 다양한 배수체로 나타났으며, x = 12의 기본염색체수를 갖는 분류군에서도 4배체, 6배체가 확인되었다. 갈퀴덩굴(G. spurium var. echinospermon (Wallr.) Hayek, 2n = 44)을 비롯하여 좀네잎갈퀴(G. gracilens (A. Gray) Makino, 2n = 22), 산갈퀴(G. pogonanthum Franch. & Sav., 2n = 22, 44), 네잎갈퀴(G. trachyspermum A. Gray, 2n = 22, 44), 검은개선갈퀴(G. japonicum (Maxim.)Makino & Nakai, 2n = 77), 개선갈퀴(G. trifloriforme Kom., 2n = 44), 큰잎갈퀴(G. dahuricum Turcz. var. dahuricum, 2n = 48, 72), 흰갈퀴(G. dahuricum var. tokyoense (Makino) Cufod., 2n = 22), 민둥갈퀴(G. kinuta Nakai & Hara, 2n = 66), 흰솔나물(G. verum var. trachycarpum for. nikkoense (Nakai) Ohwi, 2n = 44), 애기솔나물(G. verum var. asiaticum for. pusillum (Nakai) M. Park, 2n = 44) 등 11분류군의 염색체수가 본 연구를 통해 새로이 밝혀졌다. 긴잎갈퀴(G. boreale L., 2n = 22)와 솔나물(G. verum var. asiaticum Nakai for. asiaticum, 2n = 44)의 염색체수는 기존의 연구결과와 동일하였고, 가는네잎갈퀴(G. trifidum L., 2n = 22)의 염색체수는 이전의 연구 결과와 달랐다. 큰잎갈퀴와 흰갈퀴는 Sect. Leptogalium의 같은 종(G. dahuricum)에 속하지만 기본염색체수는 각각 x = 12, x = 11로차이가 났다. 체세포염색체수에서도 큰잎갈퀴는 2n = 48(4배체) 또는 2n = 72(6배체)인 반면, 흰갈퀴는 2n = 22(2배체)로 확인되어 뚜렷하게 구별되었다. 본 연구 결과 체세포염색체수는 갈퀴덩굴속의 절간 유연관계를 파악하고 분류군의 한계를 논의하는데 유용한 형질로 파악되었다.

• 한국패류학회지
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• 제4권1호
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• pp.50-54
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• 1988

The chromosome of Anodota woodiana in the Lake Uiam was analysed as using air drying technique of spermatogonial tissue to obtain mitotic and meiotic chromosomes. The chromosome chcle did mot differ, in general, from that found in other bivalves. Chromosome of this species consisted of metacentrics and submetacentrics. The longest chromosome was 2.1 ${\mu}{\textrm}{m}$ and the shortest was about 1.4 ${\mu}{\textrm}{m}$ in length.

• 식물분류학회지
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• 제35권2호
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• pp.143-151
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• 2005

한국 특산식물인 미선나무 1종을 대상으로 세포학적 조사를 수행한 결과 2n=28로 x=14의 2배수성 식물로 조사되었다. 염색체 크기는 $1.00{\mu}m$에서 $2.03{\mu}m$의 크기를 보였고, 그 크기는 연속적인 상태를 나타내었다. 본 연구에서 밝혀진 세포학적 형질인 기본염색체수, 크기의 연속성, 배수성 및 핵형에 있어 개나리속 식물과 거의 유사한 특징을 갖는 것으로 밝혀져 이들 속간에 세포학적으로 유연관계가 밀접한 것으로 판단되며, 미선나무속과 개나리속은 동일족에 포함되는 것이 타당할 것으로 사료된다.

• Asian-Australasian Journal of Animal Sciences
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• 제21권2호
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• pp.155-160
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• 2008

Several studies have reported quantitative trait loci (QTL) for meat quality on porcine chromosome 2 (http://www.animalgenome.org/QTLdb/pig.html). For application of the molecular genetic information to the pig industry through marker-assisted selection, single nucleotide polymorphism (SNP) markers were analyzed by comparative re-sequencing of polymerase chain reaction (PCR) products of 13 candidate genes with DNA from commercial pig breeds such as Berkshire, Yorkshire, Landrace, Duroc and Korean Native pig. A total of 34 SNPs were identified in 15 PCR products producing an average of one SNP in every 253 bp. PCR restriction fragment length polymorphism (RFLP) assays were developed for 11 SNPs and used to investigate allele frequencies in five commercial pig breeds in Korea. Eight of the SNPs appear to be fixed in at least one of the five pig breeds, which indicates that different selection among pig breeds might be applied to these SNPs. Polymorphisms detected in the PTH, CSF2 and FOLR genes were chosen to genotype a Berkshire-Yorkshire pig breed reference family for linkage and association analyses. Using linkage analysis, PTH and CSF2 loci were mapped to pig chromosome 2, while FOLR was mapped to pig chromosome 9. Association analyses between SNPs in the PTH, CSF2 and FOLR suggested that the CSF2 MboII polymorphism was significantly associated with several pork quality traits in the Berkshire and Yorkshire crossed F2 pigs. Our current findings provide useful SNP marker information to fine map QTL regions on pig chromosome 2 and to clarify the relevance of SNP and quantitative traits in commercial pig populations.

• 식물분류학회지
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• 제52권2호
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• pp.102-107
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• 2022

Rhododendron keiskei var. hypoglaucum (Ericaceae) was recently reported in Korea, with a disjunct distribution on the southern islands of the Korean Peninsula. Although chromosome numbers and ploidy variations are important traits in angiosperms, gaining a clear understanding the cytological features of Rhododendron has been hampered by the small size of its chromosomes. We herein report the chromosome number, karyotype structure, and genome size of R. keiskei var. hypoglaucum for the first time. The chromosome number of the investigated plants was 2n = 26 with x = 13 as the base chromosome number, which is the one of the frequently encountered base chromosome numbers in Rhododendron. The karyotype of R. keiskei var. hypoglaucum is composed of metacentric and submetacentric chromosomes similar in length, which ranged from 1.39 to 2.40 ㎛. The DNA 1C-value in all examined accessions was small, ranging from 0.63 to 0.65 pg, further supporting the stable genome size in Rhododendron. These comprehensive cytological results provide a framework for detailed molecular, cytogenetic, and phylogenomic analyses that can be used to interpret the slow species diversification rate in Rhododendron.

• 한국약용작물학회지
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• 제12권5호
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• pp.397-400
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• 2004

The chromosome numbers and karyotypes were investigated in four Korean native species of the genus Hosta. The chromosome complements were diploid of 2n=60 in H. japonica var. lancifolia Nakai and H. capitata Nakai, aneuploid of 2n=59 in H. minor (Bak.) Nakai, and modified triploid of 2n=92 in H. longipes (Fr. et Sav.) Matsumura. All the species carried four sets of distinctly large chromosomes of which the chromosome types were telocentrics or subtelocentrics with $4.4{\sim}7.2\;{\mu}m$ in length. The other chromosomes were meta-, submeta, subtelo-, or telocentric types and showed gradual length degradation in the range of $1.0{\sim}3.0\;{\mu}m$. The satellites appeared vestigially in a pair or a triplet set of chromosomes which depends on the species. New chromosome number and karyotype in H. longipes were the first report in this species. The structural rearrangement was suggested to explain the modified triploid composition of 2n=92.

• Clinical and Experimental Pediatrics
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• 제59권sup1호
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• pp.10-13
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• 2016

Chromosome 11q13 deletion syndrome has been previously reported as either otodental syndrome or oculo-oto-dental syndrome. The otodental syndrome is characterized by dental abnormalities and high-frequency sensorineural hearing loss, and by ocular coloboma in some cases. The underlying genetic defect causing otodental syndrome is a hemizygous microdeletion involving the FGF3 gene on chromosome 11q13.3. Recently, a new form of severe deafness, microtia (small ear) and small teeth, without the appearance of eye abnormalities, was also reported. In this report, we describe a 1-year-old girl presenting with ptosis of the left upper eyelid, right auricular deformity, high-arched palate, delayed dentition, simian line on the right hand, microcephaly, and developmental delay. In this patient, we identified a deletion in the chromosome 11q13.2-q13.3 (2.75 Mb) region by using an array-comparative genomic hybridization analysis. The deletion in chromosome 11q13 results in a syndrome characterized by variable clinical manifestations. Some of these manifestations involve craniofacial dysmorphology and require a functional workup for hearing, ophthalmic examinations, and long-term dental care.

• Toxicological Research
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• 제33권4호
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• pp.315-323
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• 2017

Preconceptual sex selection is still a highly debatable process whereby X- and Y-chromosome-bearing spermatozoa are isolated prior to fertilization of the oocyte. Although various separation techniques are available, none can guarantee 100% accuracy. The aim of this study was to separate X- and Y-chromosome-bearing spermatozoa using methods based on the viability difference between the X- and Y-chromosome-bearing spermatozoa. A total of 18 experimental semen samples were used, written consent was obtained from all donors and results were analysed in a blinded fashion. Spermatozoa were exposed to different pH values (5.5, 6.5, 7.5, 8.5, and 9.5), increased temperatures ($37^{\circ}C$, $41^{\circ}C$, and $45^{\circ}C$) and ROS level ($50{\mu}M$, $750{\mu}M$, and $1,000{\mu}M$). The live and dead cell separation was done through a modified swim-up technique. Changes in the sex-chromosome ratio of samples were established by double-label fluorescent in situ hybridization (FISH) before and after processing. The results indicated successful enrichment of X-chromosome-bearing spermatozoa upon incubation in acidic media, increased temperatures, and elevated $H_2O_2$. This study demonstrated the potential role for exploring the physiological differences between X-and Y-chromosome-bearing spermatozoa in the development of preconceptual gender selection.

• 한국잠사곤충학회지
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• 제3권
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• pp.59-60
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• 1963

1. 유엽의 Smear Method가 타법에 못지않게 염색체수 조사에 이용될 수 있음을 확인하였다. 2. 우리나라 재래삼은 전부가 체세포염색체수 28개의 이배체상수임을 알게 되었다. 3. 자연적으로 기상환경에 의하여 3배체상수가 생성한 일이 없었음을 증명해 주는 것이다.

• Journal of Radiation Protection and Research
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• 제24권1호
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• pp.45-53
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• 1999

각 염색체에 특이한 DNA probe를 이용하는 FISH기법은 방사선에 의해 유발된 상호전좌 및 삽입 등의 염색체의 구조적 변화를 측정하는 매우 효과적인 방법으로서 그 활용성이 증가되고 있다. 본연구는 방사선 피폭시 생물학적 선량측정법으로서 FISH기법을 활용하기 위하여 사람의 1, 2, 4번 염색체에 특이한 probe를 이용하여 고선량 단일 피폭시 유발된 각종 염색체 이상빈도를 관찰하고 이를 PAINT분류체계에 의해 분석하였다. 방사선 조사에 의한 염색체 이상빈도는 상호전좌(t)와 이동원염색체(dic)의 수가 선량 증가에 따라 같이 증가하는 것을 알 수 있으며 color junction의 수도 선량에 따라 증가하는 것을 알 수 있었다. 상호전좌의 빈도는 이동원 염색체의 빈도보다 상대적으로 높게 나타났다. 삽입(ins), 무동원염색체(ace), 및 환상염색체(r)의 수도 선량 증가에 따라 같이 증가하는 것을 알 수 있었다. 기존의 염색체재배열 분석방법과 비교해 볼 때 FISH기법은 다양한 형태의 염색체재해열을 보다 쉽게 관찰할 수 있게 하며 생물학적 선량제로서 중요한 역할을 할 것이라 기대된다.