Human chromosomal heteromorphism in American blacks. V. Racial differences in size variation of the short arm of acrocentric chromosomes

1981 ◽  
Vol 37 (3) ◽  
pp. 241-243 ◽  
Author(s):  
R. S. Verma ◽  
H. Dosik
Author(s):  
Nidhi P. Shah ◽  
Parth S. Shah ◽  
Jeanny Dominic ◽  
Bhavini S. Shah ◽  
Sandip S. Shah ◽  
...  

Background and Objectives: Human cell nucleus has, the genome consisting of euchromatin and heterochromatin. The euchromatin has gene-rich and actively functional. The heterochromatin has two components namely constitutive and facultative, where the former is highly polymorphic. It is related to numerous diseases like cancer and infertility which is now well known, though it was earlier thought to be inactive; hence the implication of these polymorphic variants of chromosomes is reviewed with respect to acrocentric and non- acrocentric types. Methodologies: The polymorphic variants can be detected by C, G, Q and R banding techniques. We usually follow G band preparation of karyotypes following World Health Organisation (WHO) manuals and their role in cancer and reproduction is reviewed. Review and Conclusion: It is emphasized that most of the p and q arms of 1, 9, 16, D and G groups and X, Y chromosomes exhibited polymorphism which are related to cancerous and infertile conditions in both sexes. Data on few non-acrocentric chromosomes like 2, 4, 8, 10, 12, 18, 19 and 20 are not available. Our review however indicated that the evaluation of specific heteromorphic variants needs to be detected using specific probes for confirmation of anomaly to assist affected cases, though earlier data indicated ambiguous information with few cases analyzed regarding assisted reproductive technologies and malignancy condition. This appraisal thus would play a key role in human chromosomal heteromorphic abnormalities and recommend genetic tests and counseling ultimately made available to the affected cases.


1998 ◽  
Vol 28 (3) ◽  
pp. 119-128 ◽  
Author(s):  
Leon J. Kamin ◽  
Safiya Omari

We review recent research which estimates racial differences in cranial capacity by measuring head dimensions of living persons. We describe errors in published reports, and find that American whites have greater head height than American blacks, but that blacks have greater head length and greater head circumference. Estimates of cranial capacity are determined by racial differences in head shape. Possible relations between head size and measured IQ are so small that they cannot possibly explain black-white differences in IQ. Why, despite this, does ‘scientific’ interest in race differences in cranial capacity persist?


Hypertension ◽  
2000 ◽  
Vol 36 (suppl_1) ◽  
pp. 715-715
Author(s):  
Lawrence J Appel ◽  
Jeanne Charleston ◽  
Paul R Conlin ◽  
Thomas P Erlinger ◽  
David W Harsha ◽  
...  

P122 In most studies, American blacks have a blunted nocturnal decline in BP compared to non-blacks. A major limitation of such analyses has been the inability to control for factors that influence BP (diet, weight, physical activity and socioeconomic status). We used data from the run-in period of the DASH feeding study to determine whether racial differences in circadian BP persist after adjusting for traditional determinants of BP. At end of run-in, a 3 week period when all participants had been fed a common diet (3 gm/d of Na, 1.7 gm/d of K), we obtained ambulatory BP. Participants (198 blacks and 156 non-blacks) had a baseline random-zero SBP <160 and DBP of 80-95 mmHg (mean 131/85 mmHg in both groups). Main results are displayed below. In summary, blacks who had the same baseline BP and who ate the same diet as non-blacks had a blunted nocturnal decline in BP, even after adjustment for other factors that influence BP. Sustained nocturnal BP may partially explain the excess burden of BP-related cardiovascular disease in blacks.


PhytoKeys ◽  
2021 ◽  
Vol 187 ◽  
pp. 207-227
Author(s):  
Elizaveta Yu. Mitrenina ◽  
Andrey S. Erst ◽  
Lorenzo Peruzzi ◽  
Mikhail V. Skaptsov ◽  
Hiroshi Ikeda ◽  
...  

Comparative karyomorphological analyses of six out of the eight white-flowered species of Eranthis sect. Shibateranthis have been carried out. All studied specimens of E. byunsanensis, E. lobulata, E. pinnatifida, and E. stellata had a somatic chromosome number 2n = 16 with basic chromosome number x = 8. On the contrary, E. tanhoensis and E. sibirica had a basic chromosome number x = 7. The specimens of E. tanhoensis were diploid with 2n = 14, while the specimens of E. sibirica were polyploid with 2n = 42. Monoploid chromosome sets of the investigated diploid species had 4–5 metacentric chromosomes and 2–4 submetacentric/subtelocentric/acrocentric chromosomes. The highest level of interchromosomal asymmetry, estimated via CVCL, was found in E. byunsanensis and E. pinnatifida. The highest levels of intrachromosomal asymmetry (MCA) and heterogeneity in centromere position (CVCI) were found in E. lobulata and E. byunsanensis, while E. sibirica had the most symmetric karyotype. A multivariate PCoA analysis of basic karyotype parameters (2n, x, THL, CVCL, MCA, and CVCI) highlighted no overlap among species accessions, which was also confirmed by LDA. The average absolute monoploid DNA content (1Cx) of the 23 investigated samples of six Eranthis species varied from 9.26 ± 0.25 pg in E. sibirica to 15.93 ± 0.32 pg in E. stellata. Overall karyological affinity was highlighted between E. lobulata and E. stellata, on one side, and between E. byunsanensis and E. pinnatifida, on the other side. Interestingly, there was no significant correlation between total haploid (monoploid) chromosome length (THL) and 1Cx values in these species.


2006 ◽  
Vol 73 ◽  
pp. 77-84 ◽  
Author(s):  
Jane E. Wright ◽  
Christine Mais ◽  
José-Luis Prieto ◽  
Brian McStay

Human ribosomal genes are located in NORs (nucleolar organizer regions) on the short arms of acrocentric chromosomes. During metaphase, previously active NORs appear as prominent chromosomal features termed secondary constrictions, which are achromatic in chromosome banding and positive in silver staining. The architectural RNA polymerase I transcription factor UBF (upstream binding factor) binds extensively across the ribosomal gene repeat throughout the cell cycle. Evidence that UBF underpins NOR structure is provided by an examination of cell lines in which large arrays of a heterologous UBF binding sequences are integrated at ectopic sites on human chromosomes. These arrays efficiently recruit UBF even to sites outside the nucleolus, and during metaphase form novel silver-stainable secondary constrictions, termed pseudo-NORs, that are morphologically similar to NORs.


2006 ◽  
Vol 175 (4S) ◽  
pp. 45-46
Author(s):  
Jacob H. Cohen ◽  
Victor J. Schoenbach ◽  
Jay S. Kaufman ◽  
James A. Talcott ◽  
Paul A. Godley

2006 ◽  
Vol 175 (4S) ◽  
pp. 68-69
Author(s):  
Nitya Abraham ◽  
Fei Wan ◽  
Chantal Montagnet ◽  
Yu-Ning Wong ◽  
Katrina Armstrong

2008 ◽  
Author(s):  
Joanna L. Goplen ◽  
E. Ashby Plant ◽  
Joyce Ehrlinger ◽  
Jonathan W. Kunstman ◽  
Corey J. Columb ◽  
...  

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