17
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Multiple changes in sialic acid biology during human evolution

      research-article
      Glycoconjugate Journal
      Springer US
      Sialic acids, Human evolution, Primates, Inflammation, N-glycolylneuraminic acid, Siglecs

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Humans are genetically very similar to “great apes”, (chimpanzees, bonobos, gorillas and orangutans), our closest evolutionary relatives. We have discovered multiple genetic and biochemical differences between humans and these other hominids, in relation to sialic acids and in Siglecs (Sia-recognizing Ig superfamily lectins). An inactivating mutation in the CMAH gene eliminated human expression of N-glycolylneuraminic acid (Neu5Gc) a major sialic acid in “great apes”. Additional human-specific changes have been found, affecting at least 10 of the <60 genes known to be involved in the biology of sialic acids. There are potential implications for unique features of humans, as well as for human susceptibility or resistance to disease. Additionally, metabolic incorporation of Neu5Gc from animal-derived materials occurs into biotherapeutic molecules and cellular preparations - and into human tissues from dietary sources, particularly red meat and milk products. As humans also have varying and sometime high levels of circulating anti-Neu5Gc antibodies, there are implications for biotechnology products, and for some human diseases associated with chronic inflammation.

          Related collections

          Most cited references122

          • Record: found
          • Abstract: found
          • Article: not found

          Structure and receptor specificity of the hemagglutinin from an H5N1 influenza virus.

          The hemagglutinin (HA) structure at 2.9 angstrom resolution, from a highly pathogenic Vietnamese H5N1 influenza virus, is more related to the 1918 and other human H1 HAs than to a 1997 duck H5 HA. Glycan microarray analysis of this Viet04 HA reveals an avian alpha2-3 sialic acid receptor binding preference. Introduction of mutations that can convert H1 serotype HAs to human alpha2-6 receptor specificity only enhanced or reduced affinity for avian-type receptors. However, mutations that can convert avian H2 and H3 HAs to human receptor specificity, when inserted onto the Viet04 H5 HA framework, permitted binding to a natural human alpha2-6 glycan, which suggests a path for this H5N1 virus to gain a foothold in the human population.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Glycan-based interactions involving vertebrate sialic-acid-recognizing proteins.

            Ajit Varki (2007)
            All cells in nature are covered by a dense and complex array of carbohydrates. Given their prominence on cell surfaces, it is not surprising that these glycans mediate and/or modulate many cellular interactions. Proteins that bind sialic acid, a sugar that is found on the surface of the cell and on secreted proteins in vertebrates, are involved in a broad range of biological processes, including intercellular adhesion, signalling and microbial attachment. Studying the roles of such proteins in vertebrates has improved our understanding of normal physiology, disease and human evolution.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Human uptake and incorporation of an immunogenic nonhuman dietary sialic acid.

              Humans are genetically unable to produce the sialic acid N-glycolylneuraminic acid (Neu5Gc), because of a mutation that occurred after our last common ancestor with great apes. Although Neu5Gc is presumed absent from normal humans, small amounts have been claimed to exist in human tumors and fetal meconium. We have generated an antibody with high specificity and avidity for Neu5Gc. Fetal tissues, normal adult tissues, and breast carcinomas from humans showed reactivity to this antibody, primarily within secretory epithelia and blood vessels. The presence of small amounts of Neu5Gc was confirmed by MS. Absent any known alternate pathway for its synthesis, we reasoned that these small amounts of Neu5Gc might originate from exogenous sources. Indeed, human cells fed with Neu5Gc incorporated it into endogenous glycoproteins. When normal human volunteers ingested Neu5Gc, a portion was absorbed and eliminated in urine, and small quantities were incorporated into newly synthesized glycoproteins. Neu5Gc has never been reported in plants or microbes to our knowledge. We found that Neu5Gc is rare in poultry and fish, common in milk products, and enriched in red meats. Furthermore, normal humans have variable amounts of circulating IgA, IgM, and IgG antibodies against Neu5Gc, with the highest levels comparable to those of the previously known anti-alpha-galactose xenoreactive antibodies. This finding represents an instance wherein humans absorb and metabolically incorporate a nonhuman dietary component enriched in foods of mammalian origin, even while generating xenoreactive, and potentially autoreactive, antibodies against the same molecule. Potential implications for human diseases are briefly discussed.
                Bookmark

                Author and article information

                Contributors
                +1-858-5342214 , +1-858-5345611 , a1varki@ucsd.edu
                Journal
                Glycoconj J
                Glycoconj. J
                Glycoconjugate Journal
                Springer US (Boston )
                0282-0080
                1573-4986
                7 September 2008
                2009
                : 26
                : 3
                : 231-245
                Affiliations
                GRID grid.266100.3, ISNI 0000000121074242, Center for Academic Research and Training in Anthropogeny, Glycobiology Research and Training Center, Departments of Medicine and Cellular and Molecular Medicine, , University of California, San Diego, ; 9500 Gilman Dr MC 0687, La Jolla, CA 92093-0687 USA
                Article
                9183
                10.1007/s10719-008-9183-z
                7087641
                18777136
                ddf69cce-b93d-4b17-8a2d-327548f2d9cc
                © Springer Science+Business Media, LLC 2008

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 11 May 2008
                : 9 August 2008
                : 18 August 2008
                Categories
                Article
                Custom metadata
                © Springer Science+Business Media, LLC 2009

                Biochemistry
                sialic acids,human evolution,primates,inflammation,n-glycolylneuraminic acid,siglecs
                Biochemistry
                sialic acids, human evolution, primates, inflammation, n-glycolylneuraminic acid, siglecs

                Comments

                Comment on this article