Chromosome-specific alpha satellites two distinct families on human chromosome 18


     Related Videos
Alpha Helix
  • Alpha Helix

  • The alpha helix is one of the most common secondary structures in proteins. This video describes the...

Alpha Epsilon Boule' Educational Foundation - Lecture Series 1 - YouTube
ALPHA STIRLING CYCLE ENGINE DIY OFF THE SHELF STEAM ENGINE SOLAR MOTOR
Specific Indications for Spine Surgery
Law 270 7 - Lecture 8 - Technology-Specific Issues and Opportunities Geothermal

     Related Hubpages

    •  Doc. Url:    Embed Code: 

    • PubMed  status
      (0) (0 Votes)
      Views: (1032)   Date: (20-01-09)   Pages: ()
    • Author:  Alexandrov IA  Mashkova TD  Akopian TA  Medvedev LI  Kisselev LL  Mitkevich SP  Yurov YB.  

    • Abstract:  Chromosome-specific alpha satellites: two distinct families on human chromosome 18. Alexandrov IA, Mashkova TD, Akopian TA, Medvedev LI, Kisselev LL, Mitkevich SP, Yurov YB. All-Union Research Center of Mental Health, Moscow, USSR. Two types of human chromosome 18-specific alpha satellite fragments have been cloned and sequenced. They represent closely related but distinct alphoid families formed by two different types of the higher-order repeated units (1360-bp EcoRI and 1700-bp HindIII fragments) that do not alternate in the genome. The individual repeats within each family are 99% identical and interfamily homology is about 78%. Sequence analysis shows that both repeats belong to alphoid suprachromosomal family 2, but their homology is not higher than that of family members located on different chromosomes. Therefore, the two repeats shared a common origin in the recent past, although they are not the direct offspring of one ancestral sequence. Our data indicate that these two 18-specific domains have appeared as a result of two separate amplification events. Despite the high degree of homology, they are not undergoing intrachromosomal homogenization, although some variation of this process might take place within each domain. PMID: 1765373 [PubMed - indexed for MEDLINE]

         Related Documents

           Related Groups

             Related Science News

               More on Sciencestage

               Answers

               News
          • Chromosome Analyses Of Prickly Pear Cacti Reveal Southern Glacial Refugia
            Analysis of chromosome number variation among species of a North American group of prickly pear cacti (nopales) showed that the most widespread species encountered are of hybrid origin. Those widespread species likely originated from hybridization among closely related parental species from western and southeastern North America. This study was published in the open access journal Comparative ...
          • OpGen Demonstrates Whole Human Chromosome Mapping Capabilities at 2012 AGBT Meeting
            OpGen, Inc., a whole-genome analysis company developing and commercializing a complete suite of break-through products and services based on its proprietary Whole Genome Mapping technology, announced today a new application for whole human chromosome mapping that improves the completeness of human genomes and enables thorough analysis of a wide spectrum of structural variations.
          • The Y Chromosome May Explain Why Men Have Earlier Coronary Disease
            The earlier onset of coronary artery disease in men has long provoked speculation and research. Now a new study in the Lancet suggests that common variations in the Y chromosome (which is transmitted directly from father to son and does not undergo recombination) may play an important role in the increased risk seen in men.
          • Heart Disease Risk May Be Tied to Y Chromosome
            Men’s higher risk for heart disease may result in part from genetic variants on the one chromosome unique to men, researchers have found.
          • Y chromosome may be the link that passes heart disease risk from father to son
            The study, published in The Lancet, focused on genetic markers on the Y chromosome — which is present only in male DNA (women have two X chromosomes) — and found that men with a certain genetic variant were 50% more likely to have coronary artery disease than those without it. The increased risk was independent of other contributors to heart disease such as age, weight, high cholesterol, high ...
          • Y Chromosome Can Raise Heart Disease Risk by 50 Percent
            Image courtesy of iStockphoto/luckyraccoon Men tend to get coronary artery disease much earlier than do women. For some men, the reason for that might be in part because of their fathers and their father’s father according to a new study , published online Wednesday in The Lancet . [More]
          • Y chromosome 'may play role in passing heart disease from father to son'
            Washington, Feb 9 (ANI): A common heart disease, which kills thousands of people each year, may be passed genetically from father to son, a new study has said.
          • Heart Disease Risk Gene May Pass From Dads to Sons
            WEDNESDAY, Feb. 8 (HealthDay News) -- An increased risk for coronary artery disease can be passed genetically from father to son on the male Y chromosome, a new study says.
          • Chimp 'X factor': Extensive adaptive evolution specifically targeting the X chromosome of chimpanzees
            Genetic mutations that boost an individual's adaptability have greater chances of getting through to X chromosomes -- at least in chimpanzees, according to new Danish research. An analysis of the genes of 12 chimpanzees has now demonstrated that the chimpanzee X chromosome plays a very special role in the animal's evolutionary development.
          • Y Chromosome Raises Heart Disease Risk By 50%, Study Shows
            Men tend to get coronary artery disease much earlier than do women. For some men, the reason for that might be in part because of their fathers--and their father's father--according to a new study , published online Wednesday in The Lancet .

               Related on Wikipedia




























           

          Powered free by PHPmotion