Evidence map›Paper›PMID 1679439›Full record

ArticleThe Journal of clinical investigation1991

Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.

T L Coetzer, K Sahr, J Prchal, H Blacklock, L Peterson, R Koler, J Doyle, J Manaster, J Palek

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 7 institutions in 5 countries.

T L CoetzerDepartment of Biomedical Research, St. Elizabeth's Hospital of Boston, Tufts University School of Medicine, Boston, Massachusetts 02135.
K Sahr
J Prchal
H Blacklock
L Peterson
R Koler
J Doyle
J Manaster
J Palek
Tufts University · USHennepin County Medical Center · USMiddlemore Hospital · NZSt. Elizabeth's Hospital · PKUniversity of Alabama · USUniversity of Toronto · CAWestern Galilee Hospital · IL

Funding

MEMBRANE SKELETON IN ABNORMAL RED CELLSR01HL027215 · NHLBI · ST. ELIZABETH'S MEDICAL CENTER OF BOSTON · PI PALEK, JIRI · 1985 to 1985
–
MEMBRANE SKELETON IN ABNORMAL RED CELLSR37HL027215 · NHLBI · ST. ELIZABETH'S MEDICAL CENTER OF BOSTON · PI PALEK, JIRI · 1986 to 1995
–
NHLBI NIH HHS HL27215NHLBI NIH HHS HL3746
6 · The paper itself

Abstract

Hereditary elliptocytosis (HE) Sp alpha I/74 is a disorder associated with defective spectrin (Sp) heterodimer self-association and an abnormal tryptic cleavage of the 80-kD alpha I domain of Sp resulting in increased amounts of a 74-kD peptide. The molecular basis of this disorder is heterogeneous and mutations in codons 28, 46, 48, and 49 (codons 22, 40, 42, and 43 in the previous nomenclature which did not include the six NH2-terminal amino acids) have been reported. In this study we present data on seven unrelated HE Sp alpha I/74 kindred from diverse racial backgrounds in whom we identified four different mutations all occurring in exon 2 of alpha Sp at codon 28. Utilizing the polymerase chain reaction we established a CGT----CTT; Arg----Leu 28 mutation in one kindred of Arab/Druze origin. In two unrelated white kindred of English/European origin the substitution is CGT----AGT; Arg----Ser 28 and in two apparently unrelated white kindred from New Zealand, the mutation is CGT----TGT; Arg----Cys 28. Finally, in one American black kindred and in a black kindred from Ghana the mutation involves CGT----CAT; Arg----His 28. Allele specific oligonucleotide hybridization confirmed that the probands are heterozygous for the respective mutant alleles. All four point mutations abolished an Aha II restriction enzyme site which allowed verification of linkage of the mutation with HE Sp alpha I/74. Our results imply that codon 28 of alpha Sp is a "hot spot" for mutations and also indicate that Arg 28 is critical for the conformational stability and functional self association of Sp heterodimers.

Indexed as

CodonMutationBase SequenceElliptocytosis, HereditaryGenetic LinkageHumansMolecular Sequence DataNucleic Acid HybridizationPolymorphism, Restriction Fragment LengthProtein ConformationSpectrinCodonSpectrin

Identifiers

PMID1679439
PMCPMC295451
OpenAlexW1978460514

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.